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<!--
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UID=11449
|
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ConceptID=C0037268
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Congenital anomaly of skin</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>11449</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0037268</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Abnormalities, Skin; Abnormality, Skin; Skin Abnormalities; Skin Abnormality</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Congenital anomaly of skin (199879009); Congenital cutaneous anomaly (199879009); Congenital malformation of the skin (199879009); Congenital skin anomalies (199879009)</td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln">A skin abnormality that is present at birth or detected in the neonatal period. [from <a title="NCI Thesaurus" href="http://ncit.nci.nih.gov" class="defSource" target="_blank">NCI</a>]</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Congenital anomaly of skin</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/871309" ref="tree=MeSH" title="MedGen record for Abnormality of prenatal development or birth">Abnormality of prenatal development or birth</a></span><ul><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><ul><li><span class="matched_ds">Congenital anomaly of skin</span><ul><li><span class="TLline"><a href="/medgen/1301" ref="tree=MeSH" title="MedGen record for Acrodermatitis">Acrodermatitis</a></span></li><li><span class="TLline"><a href="/medgen/266204" ref="tree=MeSH" title="MedGen record for Anetoderma">Anetoderma</a></span></li><li><span class="TLline"><a href="/medgen/79390" ref="tree=MeSH" title="MedGen record for Aplasia cutis congenita">Aplasia cutis congenita</a></span><ul><li><span class="TLline"><a href="/medgen/343411" ref="tree=MeSH" title="MedGen record for Aplasia cutis congenita of scalp">Aplasia cutis congenita of scalp</a></span><ul><li><span class="TLline"><a href="/medgen/350194" ref="tree=MeSH" title="MedGen record for Aplasia cutis congenita over parietal area">Aplasia cutis congenita over parietal area</a></span></li><li><span class="TLline"><a href="/medgen/370826" ref="tree=MeSH" title="MedGen record for Aplasia cutis congenita over the scalp vertex">Aplasia cutis congenita over the scalp vertex</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/400308" ref="tree=MeSH" title="MedGen record for Aplasia cutis congenita on trunk or limbs">Aplasia cutis congenita on trunk or limbs</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/140810" ref="tree=MeSH" title="MedGen record for Carney complex">Carney complex</a></span><ul><li><span class="TLline"><a href="/medgen/340253" ref="tree=MeSH" title="MedGen record for Carney complex type 2">Carney complex type 2</a></span></li><li><span class="TLline"><a href="/medgen/388559" ref="tree=MeSH" title="MedGen record for Carney complex, type 1">Carney complex, type 1</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/78580" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita">Dyskeratosis congenita</a></span><ul><li><span class="TLline"><a href="/medgen/502504" ref="tree=MeSH" title="MedGen record for Autosomal recessive dyskeratosis congenita">Autosomal recessive dyskeratosis congenita</a></span><ul><li><span class="TLline"><a href="/medgen/341705" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal recessive 1">Dyskeratosis congenita, autosomal recessive 1</a></span></li><li><span class="TLline"><a href="/medgen/462791" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal recessive 2">Dyskeratosis congenita, autosomal recessive 2</a></span></li><li><span class="TLline"><a href="/medgen/462792" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal recessive 3">Dyskeratosis congenita, autosomal recessive 3</a></span></li><li><span class="TLline"><a href="/medgen/905452" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal recessive 6">Dyskeratosis congenita, autosomal recessive 6</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/462794" ref="tree=MeSH" title="MedGen record for Autosomal recessive dyskeratosis congenita 4">Autosomal recessive dyskeratosis congenita 4</a></span></li><li><span class="TLline"><a href="/medgen/1645250" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal dominant 1">Dyskeratosis congenita, autosomal dominant 1</a></span><ul><li><span class="TLline"><a href="/medgen/462793" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal dominant 2">Dyskeratosis congenita, autosomal dominant 2</a></span></li><li><span class="TLline"><a href="/medgen/462795" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal dominant 3">Dyskeratosis congenita, autosomal dominant 3</a></span></li><li><span class="TLline"><a href="/medgen/815132" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal dominant 4">Dyskeratosis congenita, autosomal dominant 4</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/904824" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal dominant 6">Dyskeratosis congenita, autosomal dominant 6</a></span></li><li><span class="TLline"><a href="/medgen/767570" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, autosomal recessive 5">Dyskeratosis congenita, autosomal recessive 5</a></span></li><li><span class="TLline"><a href="/medgen/216941" ref="tree=MeSH" title="MedGen record for Dyskeratosis congenita, X-linked">Dyskeratosis congenita, X-linked</a></span></li><li><span class="TLline"><a href="/medgen/231230" ref="tree=MeSH" title="MedGen record for Revesz syndrome">Revesz syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/8544" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia">Ectodermal dysplasia</a></span><ul><li><span class="TLline"><a href="/medgen/395426" ref="tree=MeSH" title="MedGen record for Ackerman syndrome">Ackerman syndrome</a></span></li><li><span class="TLline"><a href="/medgen/87435" ref="tree=MeSH" title="MedGen record for Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes">Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes</a></span></li><li><span class="TLline"><a href="/medgen/167081" ref="tree=MeSH" title="MedGen record for Alopecia - contractures - dwarfism - intellectual disability syndrome">Alopecia - contractures - dwarfism - intellectual disability syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98036" ref="tree=MeSH" title="MedGen record for Amelocerebrohypohidrotic syndrome">Amelocerebrohypohidrotic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/400184" ref="tree=MeSH" title="MedGen record for Ameloonychohypohidrotic syndrome">Ameloonychohypohidrotic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/310309" ref="tree=MeSH" title="MedGen record for Anhidrotic ectodermal dysplasia">Anhidrotic ectodermal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/929406" ref="tree=MeSH" title="MedGen record for Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome">Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98032" ref="tree=MeSH" title="MedGen record for Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome">Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/400148" ref="tree=MeSH" title="MedGen record for Ankyloblepharon filiforme adnatum-cleft palate syndrome">Ankyloblepharon filiforme adnatum-cleft palate syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1666000" ref="tree=MeSH" title="MedGen record for Ankyloblepharon filiforme-imperforate anus syndrome">Ankyloblepharon filiforme-imperforate anus syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/400144" ref="tree=MeSH" title="MedGen record for Anonychia with flexural pigmentation">Anonychia with flexural pigmentation</a></span></li><li><span class="TLline"><a href="/medgen/340124" ref="tree=MeSH" title="MedGen record for Arrhythmogenic cardiomyopathy with wooly hair and keratoderma">Arrhythmogenic cardiomyopathy with wooly hair and keratoderma</a></span></li><li><span class="TLline"><a href="/medgen/1674099" ref="tree=MeSH" title="MedGen record for Arthrogryposis-ectodermal dysplasia-other anomalies syndrome">Arthrogryposis-ectodermal dysplasia-other anomalies syndrome</a></span></li><li><span class="TLline"><a href="/medgen/930338" ref="tree=MeSH" title="MedGen record for Autosomal dominant palmoplantar keratoderma and congenital alopecia">Autosomal dominant palmoplantar keratoderma and congenital alopecia</a></span></li><li><span class="TLline"><a href="/medgen/96067" ref="tree=MeSH" title="MedGen record for Autosomal recessive hypohidrotic ectodermal dysplasia syndrome">Autosomal recessive hypohidrotic ectodermal dysplasia syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/854356" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive">Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive</a></span></li><li><span class="TLline"><a href="/medgen/761671" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive">Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive</a></span></li><li><span class="TLline"><a href="/medgen/1680605" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia 15, hypohidrotic/hair type">Ectodermal dysplasia 15, hypohidrotic/hair type</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/347851" ref="tree=MeSH" title="MedGen record for Autosomal recessive palmoplantar keratoderma and congenital alopecia">Autosomal recessive palmoplantar keratoderma and congenital alopecia</a></span></li><li><span class="TLline"><a href="/medgen/230818" ref="tree=MeSH" title="MedGen record for Barber-Say syndrome">Barber-Say syndrome</a></span></li><li><span class="TLline"><a href="/medgen/337894" ref="tree=MeSH" title="MedGen record for Bartsocas-Papas syndrome 1">Bartsocas-Papas syndrome 1</a></span></li><li><span class="TLline"><a href="/medgen/349302" ref="tree=MeSH" title="MedGen record for Blepharocheilodontic syndrome">Blepharocheilodontic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/266149" ref="tree=MeSH" title="MedGen record for Cardio-facio-cutaneous syndrome">Cardio-facio-cutaneous syndrome</a></span></li><li><span class="TLline"><a href="/medgen/167117" ref="tree=MeSH" title="MedGen record for Cataract-hypertrichosis-intellectual disability syndrome">Cataract-hypertrichosis-intellectual disability syndrome</a></span></li><li><span class="TLline"><a href="/medgen/347850" ref="tree=MeSH" title="MedGen record for Cerebellar ataxia-ectodermal dysplasia syndrome">Cerebellar ataxia-ectodermal dysplasia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/341214" ref="tree=MeSH" title="MedGen record for CHIME syndrome">CHIME syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1641815" ref="tree=MeSH" title="MedGen record for Chondroectodermal dysplasia with night blindness">Chondroectodermal dysplasia with night blindness</a></span></li><li><span class="TLline"><a href="/medgen/419316" ref="tree=MeSH" title="MedGen record for Choroidal atrophy-alopecia syndrome">Choroidal atrophy-alopecia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/444067" ref="tree=MeSH" title="MedGen record for Cleft lip/palate-ectodermal dysplasia syndrome">Cleft lip/palate-ectodermal dysplasia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/347428" ref="tree=MeSH" title="MedGen record for Conductive deafness-ptosis-skeletal anomalies syndrome">Conductive deafness-ptosis-skeletal anomalies syndrome</a></span></li><li><span class="TLline"><a href="/medgen/316921" ref="tree=MeSH" title="MedGen record for Congenital hypotrichosis with juvenile macular dystrophy">Congenital hypotrichosis with juvenile macular dystrophy</a></span></li><li><span class="TLline"><a href="/medgen/375546" ref="tree=MeSH" title="MedGen record for Contractures-ectodermal dysplasia-cleft lip/palate syndrome">Contractures-ectodermal dysplasia-cleft lip/palate syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1641011" ref="tree=MeSH" title="MedGen record for Cranioectodermal dysplasia">Cranioectodermal dysplasia</a></span><ul><li><span class="TLline"><a href="/medgen/96586" ref="tree=MeSH" title="MedGen record for Cranioectodermal dysplasia 1">Cranioectodermal dysplasia 1</a></span></li><li><span class="TLline"><a href="/medgen/462224" ref="tree=MeSH" title="MedGen record for Cranioectodermal dysplasia 2">Cranioectodermal dysplasia 2</a></span></li><li><span class="TLline"><a href="/medgen/481437" ref="tree=MeSH" title="MedGen record for Cranioectodermal dysplasia 3">Cranioectodermal dysplasia 3</a></span></li><li><span class="TLline"><a href="/medgen/482246" ref="tree=MeSH" title="MedGen record for Cranioectodermal dysplasia 4">Cranioectodermal dysplasia 4</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/129128" ref="tree=MeSH" title="MedGen record for Cronkhite-Canada syndrome">Cronkhite-Canada syndrome</a></span></li><li><span class="TLline"><a href="/medgen/335923" ref="tree=MeSH" title="MedGen record for Curly hair - acral keratoderma - caries syndrome">Curly hair - acral keratoderma - caries syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98035" ref="tree=MeSH" title="MedGen record for Curly hair, ankyloblepharon, nail dysplasia syndrome">Curly hair, ankyloblepharon, nail dysplasia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/141594" ref="tree=MeSH" title="MedGen record for Curry-Hall syndrome">Curry-Hall syndrome</a></span></li><li><span class="TLline"><a href="/medgen/383693" ref="tree=MeSH" title="MedGen record for Dahlberg-Borer-Newcomer syndrome">Dahlberg-Borer-Newcomer syndrome</a></span></li><li><span class="TLline"><a href="/medgen/343498" ref="tree=MeSH" title="MedGen record for Deafness, enamel hypoplasia, nail defect syndrome">Deafness, enamel hypoplasia, nail defect syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/1647369" ref="tree=MeSH" title="MedGen record for Heimler syndrome 1">Heimler syndrome 1</a></span></li><li><span class="TLline"><a href="/medgen/903520" ref="tree=MeSH" title="MedGen record for Heimler syndrome 2">Heimler syndrome 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/419158" ref="tree=MeSH" title="MedGen record for Dennis-Fairhurst-Moore syndrome">Dennis-Fairhurst-Moore syndrome</a></span></li><li><span class="TLline"><a href="/medgen/341742" ref="tree=MeSH" title="MedGen record for Dermatoosteolysis, Kirghizian type">Dermatoosteolysis, Kirghizian type</a></span></li><li><span class="TLline"><a href="/medgen/98037" ref="tree=MeSH" title="MedGen record for Dermatopathia pigmentosa reticularis">Dermatopathia pigmentosa reticularis</a></span></li><li><span class="TLline"><a href="/medgen/377602" ref="tree=MeSH" title="MedGen record for Dermo-odonto dysplasia">Dermo-odonto dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/1672480" ref="tree=MeSH" title="MedGen record for Dermotrichic syndrome">Dermotrichic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/59797" ref="tree=MeSH" title="MedGen record for Dubowitz syndrome">Dubowitz syndrome</a></span></li><li><span class="TLline"><a href="/medgen/764338" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia 8, hair/tooth/nail type">Ectodermal dysplasia 8, hair/tooth/nail type</a></span></li><li><span class="TLline"><a href="/medgen/375786" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia and immune deficiency">Ectodermal dysplasia and immune deficiency</a></span><ul><li><span class="TLline"><a href="/medgen/375787" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia and immunodeficiency 1">Ectodermal dysplasia and immunodeficiency 1</a></span></li><li><span class="TLline"><a href="/medgen/394295" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia and immunodeficiency 2">Ectodermal dysplasia and immunodeficiency 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/371331" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia with natal teeth, Turnpenny type">Ectodermal dysplasia with natal teeth, Turnpenny type</a></span></li><li><span class="TLline"><a href="/medgen/314095" ref="tree=MeSH" title="MedGen record for Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant">Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant</a></span></li><li><span class="TLline"><a href="/medgen/338798" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia, trichoodontoonychial type">Ectodermal dysplasia, trichoodontoonychial type</a></span></li><li><span class="TLline"><a href="/medgen/340297" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia-blindness syndrome">Ectodermal dysplasia-blindness syndrome</a></span></li><li><span class="TLline"><a href="/medgen/462159" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia-cutaneous syndactyly syndrome">Ectodermal dysplasia-cutaneous syndactyly syndrome</a></span></li><li><span class="TLline"><a href="/medgen/347363" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome">Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome</a></span></li><li><span class="TLline"><a href="/medgen/346503" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia-sensorineural deafness syndrome">Ectodermal dysplasia-sensorineural deafness syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1648397" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia-syndactyly syndrome">Ectodermal dysplasia-syndactyly syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98357" ref="tree=MeSH" title="MedGen record for Ectrodactyly-ectodermal dysplasia-clefting syndrome">Ectrodactyly-ectodermal dysplasia-clefting syndrome</a></span></li><li><span class="TLline"><a href="/medgen/341679" ref="tree=MeSH" title="MedGen record for EEM syndrome">EEM syndrome</a></span></li><li><span class="TLline"><a href="/medgen/8584" ref="tree=MeSH" title="MedGen record for Ellis-van Creveld syndrome">Ellis-van Creveld syndrome</a></span></li><li><span class="TLline"><a href="/medgen/388032" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa simplex due to plakophilin deficiency">Epidermolysis bullosa simplex due to plakophilin deficiency</a></span></li><li><span class="TLline"><a href="/medgen/42055" ref="tree=MeSH" title="MedGen record for Focal dermal hypoplasia">Focal dermal hypoplasia</a></span></li><li><span class="TLline"><a href="/medgen/445408" ref="tree=MeSH" title="MedGen record for Focal facial dermal dysplasia">Focal facial dermal dysplasia</a></span><ul><li><span class="TLline"><a href="/medgen/1718224" ref="tree=MeSH" title="MedGen record for Focal facial dermal dysplasia type I">Focal facial dermal dysplasia type I</a></span></li><li><span class="TLline"><a href="/medgen/767159" ref="tree=MeSH" title="MedGen record for Focal facial dermal dysplasia type II">Focal facial dermal dysplasia type II</a></span></li><li><span class="TLline"><a href="/medgen/315643" ref="tree=MeSH" title="MedGen record for Focal facial dermal dysplasia type III">Focal facial dermal dysplasia type III</a></span></li><li><span class="TLline"><a href="/medgen/767160" ref="tree=MeSH" title="MedGen record for Focal facial dermal dysplasia type IV">Focal facial dermal dysplasia type IV</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/394125" ref="tree=MeSH" title="MedGen record for Fontaine progeroid syndrome">Fontaine progeroid syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98034" ref="tree=MeSH" title="MedGen record for GAPO syndrome">GAPO syndrome</a></span></li><li><span class="TLline"><a href="/medgen/342675" ref="tree=MeSH" title="MedGen record for Gingival fibromatosis-hypertrichosis syndrome">Gingival fibromatosis-hypertrichosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/5414" ref="tree=MeSH" title="MedGen record for Hallermann-Streiff syndrome">Hallermann-Streiff syndrome</a></span></li><li><span class="TLline"><a href="/medgen/56416" ref="tree=MeSH" title="MedGen record for Hidrotic ectodermal dysplasia syndrome">Hidrotic ectodermal dysplasia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/371322" ref="tree=MeSH" title="MedGen record for Hidrotic ectodermal dysplasia, Christianson-Fourie type">Hidrotic ectodermal dysplasia, Christianson-Fourie type</a></span></li><li><span class="TLline"><a href="/medgen/443941" ref="tree=MeSH" title="MedGen record for Hidrotic ectodermal dysplasia, Halal type">Hidrotic ectodermal dysplasia, Halal type</a></span></li><li><span class="TLline"><a href="/medgen/99140" ref="tree=MeSH" title="MedGen record for Hyperhidrosis, premature cavities and premolar aplasia">Hyperhidrosis, premature cavities and premolar aplasia</a></span></li><li><span class="TLline"><a href="/medgen/870835" ref="tree=MeSH" title="MedGen record for Hypertrichosis cubiti-short stature syndrome">Hypertrichosis cubiti-short stature syndrome</a></span></li><li><span class="TLline"><a href="/medgen/66727" ref="tree=MeSH" title="MedGen record for Hypertrichosis lanuginosa congenita">Hypertrichosis lanuginosa congenita</a></span><ul><li><span class="TLline"><a href="/medgen/333542" ref="tree=MeSH" title="MedGen record for Ambras type hypertrichosis universalis congenita">Ambras type hypertrichosis universalis congenita</a></span></li><li><span class="TLline"><a href="/medgen/1856186" ref="tree=MeSH" title="MedGen record for X-linked congenital generalized hypertrichosis">X-linked congenital generalized hypertrichosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1853123" ref="tree=MeSH" title="MedGen record for Hypohidrotic ectodermal dysplasia">Hypohidrotic ectodermal dysplasia</a></span><ul><li><span class="TLline"><a href="/medgen/539190" ref="tree=MeSH" title="MedGen record for Autosomal dominant hypohidrotic ectodermal dysplasia">Autosomal dominant hypohidrotic ectodermal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/468426" ref="tree=MeSH" title="MedGen record for Autosomal hypohidrotic ectodermal dysplasia">Autosomal hypohidrotic ectodermal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/57890" ref="tree=MeSH" title="MedGen record for Hypohidrotic X-linked ectodermal dysplasia">Hypohidrotic X-linked ectodermal dysplasia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/384046" ref="tree=MeSH" title="MedGen record for Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome">Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/140809" ref="tree=MeSH" title="MedGen record for Hypoplastic enamel-onycholysis-hypohidrosis syndrome">Hypoplastic enamel-onycholysis-hypohidrosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1371854" ref="tree=MeSH" title="MedGen record for Hypotrichosis-intellectual disability, Lopes type">Hypotrichosis-intellectual disability, Lopes type</a></span></li><li><span class="TLline"><a href="/medgen/375146" ref="tree=MeSH" title="MedGen record for Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome">Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome</a></span></li><li><span class="TLline"><a href="/medgen/344577" ref="tree=MeSH" title="MedGen record for Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome">Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome</a></span></li><li><span class="TLline"><a href="/medgen/7049" ref="tree=MeSH" title="MedGen record for Incontinentia pigmenti syndrome">Incontinentia pigmenti syndrome</a></span></li><li><span class="TLline"><a href="/medgen/59798" ref="tree=MeSH" title="MedGen record for Johanson-Blizzard syndrome">Johanson-Blizzard syndrome</a></span></li><li><span class="TLline"><a href="/medgen/167092" ref="tree=MeSH" title="MedGen record for Johnson neuroectodermal syndrome">Johnson neuroectodermal syndrome</a></span></li><li><span class="TLline"><a href="/medgen/777082" ref="tree=MeSH" title="MedGen record for Keratitis ichthyosis and deafness syndrome">Keratitis ichthyosis and deafness syndrome</a></span></li><li><span class="TLline"><a href="/medgen/334042" ref="tree=MeSH" title="MedGen record for Lelis syndrome">Lelis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/383698" ref="tree=MeSH" title="MedGen record for Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome">Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1806249" ref="tree=MeSH" title="MedGen record for Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies">Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies</a></span></li><li><span class="TLline"><a href="/medgen/82694" ref="tree=MeSH" title="MedGen record for Marshall syndrome">Marshall syndrome</a></span></li><li><span class="TLline"><a href="/medgen/67398" ref="tree=MeSH" title="MedGen record for Metaphyseal chondrodysplasia, McKusick type">Metaphyseal chondrodysplasia, McKusick type</a></span></li><li><span class="TLline"><a href="/medgen/91010" ref="tree=MeSH" title="MedGen record for Naegeli-Franceschetti-Jadassohn syndrome">Naegeli-Franceschetti-Jadassohn syndrome</a></span></li><li><span class="TLline"><a href="/medgen/863424" ref="tree=MeSH" title="MedGen record for Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome">Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome</a></span></li><li><span class="TLline"><a href="/medgen/82706" ref="tree=MeSH" title="MedGen record for Neurocutaneous syndrome">Neurocutaneous syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/439" ref="tree=MeSH" title="MedGen record for Ataxia-telangiectasia syndrome">Ataxia-telangiectasia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/2554" ref="tree=MeSH" title="MedGen record for Gorlin syndrome">Gorlin syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1646345" ref="tree=MeSH" title="MedGen record for Linear nevus sebaceous syndrome">Linear nevus sebaceous syndrome</a></span></li><li><span class="TLline"><a href="/medgen/58149" ref="tree=MeSH" title="MedGen record for Neurofibromatosis">Neurofibromatosis</a></span></li><li><span class="TLline"><a href="/medgen/21361" ref="tree=MeSH" title="MedGen record for Sturge-Weber syndrome">Sturge-Weber syndrome</a></span></li><li><span class="TLline"><a href="/medgen/22518" ref="tree=MeSH" title="MedGen record for Tuberous sclerosis syndrome">Tuberous sclerosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/42458" ref="tree=MeSH" title="MedGen record for Von Hippel-Lindau syndrome">Von Hippel-Lindau syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/167236" ref="tree=MeSH" title="MedGen record for Oculodentodigital dysplasia">Oculodentodigital dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/347867" ref="tree=MeSH" title="MedGen record for Oculoosteocutaneous syndrome">Oculoosteocutaneous syndrome</a></span></li><li><span class="TLline"><a href="/medgen/340517" ref="tree=MeSH" title="MedGen record for Oculotrichodysplasia">Oculotrichodysplasia</a></span></li><li><span class="TLline"><a href="/medgen/1648007" ref="tree=MeSH" title="MedGen record for Odonto-onycho dysplasia-alopecia syndrome">Odonto-onycho dysplasia-alopecia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/208666" ref="tree=MeSH" title="MedGen record for Odonto-onycho-dermal dysplasia">Odonto-onycho-dermal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/400891" ref="tree=MeSH" title="MedGen record for Odonto-tricho-ungual-digito-palmar syndrome">Odonto-tricho-ungual-digito-palmar syndrome</a></span></li><li><span class="TLline"><a href="/medgen/443944" ref="tree=MeSH" title="MedGen record for Odontotrichomelic syndrome">Odontotrichomelic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/307142" ref="tree=MeSH" title="MedGen record for Orofaciodigital syndrome I">Orofaciodigital syndrome I</a></span></li><li><span class="TLline"><a href="/medgen/78556" ref="tree=MeSH" title="MedGen record for Pachyonychia congenita syndrome">Pachyonychia congenita syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/353335" ref="tree=MeSH" title="MedGen record for Pachyonychia congenita 1">Pachyonychia congenita 1</a></span></li><li><span class="TLline"><a href="/medgen/314107" ref="tree=MeSH" title="MedGen record for Pachyonychia congenita 2">Pachyonychia congenita 2</a></span></li><li><span class="TLline"><a href="/medgen/811523" ref="tree=MeSH" title="MedGen record for Pachyonychia congenita 3">Pachyonychia congenita 3</a></span></li><li><span class="TLline"><a href="/medgen/811524" ref="tree=MeSH" title="MedGen record for Pachyonychia congenita 4">Pachyonychia congenita 4</a></span></li><li><span class="TLline"><a href="/medgen/75476" ref="tree=MeSH" title="MedGen record for Steatocystoma multiplex">Steatocystoma multiplex</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/45306" ref="tree=MeSH" title="MedGen record for Papillon-Lefèvre syndrome">Papillon-Lefèvre syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1807813" ref="tree=MeSH" title="MedGen record for Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome">Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome</a></span></li><li><span class="TLline"><a href="/medgen/419090" ref="tree=MeSH" title="MedGen record for Pili torti-onychodysplasia syndrome">Pili torti-onychodysplasia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/376661" ref="tree=MeSH" title="MedGen record for Pilodental dysplasia-refractive errors syndrome">Pilodental dysplasia-refractive errors syndrome</a></span></li><li><span class="TLline"><a href="/medgen/978375" ref="tree=MeSH" title="MedGen record for Pure hair and nail ectodermal dysplasia">Pure hair and nail ectodermal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/357183" ref="tree=MeSH" title="MedGen record for Scalp-ear-nipple syndrome">Scalp-ear-nipple syndrome</a></span></li><li><span class="TLline"><a href="/medgen/347366" ref="tree=MeSH" title="MedGen record for SchC6pf-Schulz-Passarge syndrome">SchC6pf-Schulz-Passarge syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120517" ref="tree=MeSH" title="MedGen record for Schinzel-Giedion syndrome">Schinzel-Giedion syndrome</a></span></li><li><span class="TLline"><a href="/medgen/342260" ref="tree=MeSH" title="MedGen record for Stern-Lubinsky-Durrie syndrome">Stern-Lubinsky-Durrie syndrome</a></span></li><li><span class="TLline"><a href="/medgen/376472" ref="tree=MeSH" title="MedGen record for Teebi-Shaltout syndrome">Teebi-Shaltout syndrome</a></span></li><li><span class="TLline"><a href="/medgen/348284" ref="tree=MeSH" title="MedGen record for Thumb deformity-alopecia-pigmentation anomaly syndrome">Thumb deformity-alopecia-pigmentation anomaly syndrome</a></span></li><li><span class="TLline"><a href="/medgen/333068" ref="tree=MeSH" title="MedGen record for Toriello-Lacassie-Droste syndrome">Toriello-Lacassie-Droste syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78555" ref="tree=MeSH" title="MedGen record for Tricho-dento-osseous syndrome">Tricho-dento-osseous syndrome</a></span></li><li><span class="TLline"><a href="/medgen/96068" ref="tree=MeSH" title="MedGen record for Trichodental syndrome">Trichodental syndrome</a></span></li><li><span class="TLline"><a href="/medgen/419092" ref="tree=MeSH" title="MedGen record for Trichodermodysplasia-dental alterations syndrome">Trichodermodysplasia-dental alterations syndrome</a></span></li><li><span class="TLline"><a href="/medgen/930013" ref="tree=MeSH" title="MedGen record for Trichodysplasia-amelogenesis imperfecta syndrome">Trichodysplasia-amelogenesis imperfecta syndrome</a></span></li><li><span class="TLline"><a href="/medgen/338532" ref="tree=MeSH" title="MedGen record for Trichomegaly-retina pigmentary degeneration-dwarfism syndrome">Trichomegaly-retina pigmentary degeneration-dwarfism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/481087" ref="tree=MeSH" title="MedGen record for Trichoodontoonychial dysplasia">Trichoodontoonychial dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/363064" ref="tree=MeSH" title="MedGen record for Trichothiodystrophy">Trichothiodystrophy</a></span><ul><li><span class="TLline"><a href="/medgen/355730" ref="tree=MeSH" title="MedGen record for Trichothiodystrophy 1, photosensitive">Trichothiodystrophy 1, photosensitive</a></span></li><li><span class="TLline"><a href="/medgen/905904" ref="tree=MeSH" title="MedGen record for Trichothiodystrophy 2, photosensitive">Trichothiodystrophy 2, photosensitive</a></span></li><li><span class="TLline"><a href="/medgen/865608" ref="tree=MeSH" title="MedGen record for Trichothiodystrophy 3, photosensitive">Trichothiodystrophy 3, photosensitive</a></span></li><li><span class="TLline"><a href="/medgen/272036" ref="tree=MeSH" title="MedGen record for Trichothiodystrophy 4, nonphotosensitive">Trichothiodystrophy 4, nonphotosensitive</a></span></li><li><span class="TLline"><a href="/medgen/1684762" ref="tree=MeSH" title="MedGen record for Trichothiodystrophy 7, nonphotosensitive">Trichothiodystrophy 7, nonphotosensitive</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/348658" ref="tree=MeSH" title="MedGen record for Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome">Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome</a></span></li><li><span class="TLline"><a href="/medgen/375148" ref="tree=MeSH" title="MedGen record for Woolly hair-skin fragility syndrome">Woolly hair-skin fragility syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/41720" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome">Ehlers-Danlos syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/78662" ref="tree=MeSH" title="MedGen record for Arthrochalasia Ehlers-Danlos syndrome">Arthrochalasia Ehlers-Danlos syndrome</a></span></li><li><span class="TLline"><a href="/medgen/907426" ref="tree=MeSH" title="MedGen record for Bethlem myopathy 2">Bethlem myopathy 2</a></span></li><li><span class="TLline"><a href="/medgen/946156" ref="tree=MeSH" title="MedGen record for Brittle cornea syndrome">Brittle cornea syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/78661" ref="tree=MeSH" title="MedGen record for Brittle cornea syndrome 1">Brittle cornea syndrome 1</a></span></li><li><span class="TLline"><a href="/medgen/481641" ref="tree=MeSH" title="MedGen record for Brittle cornea syndrome 2">Brittle cornea syndrome 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/336244" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome due to tenascin-X deficiency">Ehlers-Danlos syndrome due to tenascin-X deficiency</a></span></li><li><span class="TLline"><a href="/medgen/1841549" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome progeroid type">Ehlers-Danlos syndrome progeroid type</a></span><ul><li><span class="TLline"><a href="/medgen/393515" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, spondylocheirodysplastic type">Ehlers-Danlos syndrome, spondylocheirodysplastic type</a></span></li><li><span class="TLline"><a href="/medgen/1646889" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, spondylodysplastic type, 1">Ehlers-Danlos syndrome, spondylodysplastic type, 1</a></span></li><li><span class="TLline"><a href="/medgen/815540" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, spondylodysplastic type, 2">Ehlers-Danlos syndrome, spondylodysplastic type, 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1645042" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, arthrochalasia type">Ehlers-Danlos syndrome, arthrochalasia type</a></span><ul><li><span class="TLline"><a href="/medgen/854083" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome type 7A">Ehlers-Danlos syndrome type 7A</a></span></li><li><span class="TLline"><a href="/medgen/342092" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome type 7B">Ehlers-Danlos syndrome type 7B</a></span></li><li><span class="TLline"><a href="/medgen/397792" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, dermatosparaxis type">Ehlers-Danlos syndrome, dermatosparaxis type</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/929458" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, cardiac valvular type">Ehlers-Danlos syndrome, cardiac valvular type</a></span></li><li><span class="TLline"><a href="/medgen/909864" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, classic type">Ehlers-Danlos syndrome, classic type</a></span><ul><li><span class="TLline"><a href="/medgen/78660" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, classic type, 1">Ehlers-Danlos syndrome, classic type, 1</a></span></li><li><span class="TLline"><a href="/medgen/120628" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, classic type, 2">Ehlers-Danlos syndrome, classic type, 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1632001" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, classic-like, 2">Ehlers-Danlos syndrome, classic-like, 2</a></span></li><li><span class="TLline"><a href="/medgen/75672" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, kyphoscoliotic type 1">Ehlers-Danlos syndrome, kyphoscoliotic type 1</a></span></li><li><span class="TLline"><a href="/medgen/356497" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, musculocontractural type">Ehlers-Danlos syndrome, musculocontractural type</a></span></li><li><span class="TLline"><a href="/medgen/82791" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, periodontitis type">Ehlers-Danlos syndrome, periodontitis type</a></span><ul><li><span class="TLline"><a href="/medgen/1642148" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, periodontal type 1">Ehlers-Danlos syndrome, periodontal type 1</a></span></li><li><span class="TLline"><a href="/medgen/934648" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, periodontal type 2">Ehlers-Danlos syndrome, periodontal type 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/75670" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, type 3">Ehlers-Danlos syndrome, type 3</a></span></li><li><span class="TLline"><a href="/medgen/82790" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, type 4">Ehlers-Danlos syndrome, type 4</a></span><ul><li><span class="TLline"><a href="/medgen/541287" ref="tree=MeSH" title="MedGen record for Autosomal recessive Ehlers-Danlos syndrome, vascular type">Autosomal recessive Ehlers-Danlos syndrome, vascular type</a></span></li><li><span class="TLline"><a href="/medgen/541286" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, dominant type 4">Ehlers-Danlos syndrome, dominant type 4</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1639430" ref="tree=MeSH" title="MedGen record for Kyphoscoliotic Ehlers-Danlos syndrome">Kyphoscoliotic Ehlers-Danlos syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/482790" ref="tree=MeSH" title="MedGen record for Ehlers-Danlos syndrome, kyphoscoliotic type, 2">Ehlers-Danlos syndrome, kyphoscoliotic type, 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1814455" ref="tree=MeSH" title="MedGen record for Spondylodysplastic Ehlers-Danlos syndrome">Spondylodysplastic Ehlers-Danlos syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75671" ref="tree=MeSH" title="MedGen record for X-linked Ehlers-Danlos syndrome">X-linked Ehlers-Danlos syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/41832" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa">Epidermolysis bullosa</a></span><ul><li><span class="TLline"><a href="/medgen/37178" ref="tree=MeSH" title="MedGen record for Acquired epidermolysis bullosa">Acquired epidermolysis bullosa</a></span></li><li><span class="TLline"><a href="/medgen/37179" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa dystrophica">Epidermolysis bullosa dystrophica</a></span><ul><li><span class="TLline"><a href="/medgen/266151" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa pruriginosa">Epidermolysis bullosa pruriginosa</a></span></li><li><span class="TLline"><a href="/medgen/140935" ref="tree=MeSH" title="MedGen record for Generalized dominant dystrophic epidermolysis bullosa">Generalized dominant dystrophic epidermolysis bullosa</a></span></li><li><span class="TLline"><a href="/medgen/634276" ref="tree=MeSH" title="MedGen record for Localized dystrophic epidermolysis bullosa">Localized dystrophic epidermolysis bullosa</a></span></li><li><span class="TLline"><a href="/medgen/36311" ref="tree=MeSH" title="MedGen record for Recessive dystrophic epidermolysis bullosa">Recessive dystrophic epidermolysis bullosa</a></span></li><li><span class="TLline"><a href="/medgen/698413" ref="tree=MeSH" title="MedGen record for Recessive dystrophic epidermolysis bullosa inversa">Recessive dystrophic epidermolysis bullosa inversa</a></span></li><li><span class="TLline"><a href="/medgen/1392226" ref="tree=MeSH" title="MedGen record for Recessive dystrophic epidermolysis bullosa-generalized other">Recessive dystrophic epidermolysis bullosa-generalized other</a></span></li><li><span class="TLline"><a href="/medgen/343607" ref="tree=MeSH" title="MedGen record for Transient bullous dermolysis of the newborn">Transient bullous dermolysis of the newborn</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/86896" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa simplex">Epidermolysis bullosa simplex</a></span><ul><li><span class="TLline"><a href="/medgen/38194" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa simplex 1A, generalized severe">Epidermolysis bullosa simplex 1A, generalized severe</a></span></li><li><span class="TLline"><a href="/medgen/87016" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa simplex 1C, localized">Epidermolysis bullosa simplex 1C, localized</a></span></li><li><span class="TLline"><a href="/medgen/140934" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa simplex with mottled pigmentation">Epidermolysis bullosa simplex with mottled pigmentation</a></span></li><li><span class="TLline"><a href="/medgen/1794134" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa simplex, Koebner type">Epidermolysis bullosa simplex, Koebner type</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/86898" ref="tree=MeSH" title="MedGen record for Junctional epidermolysis bullosa">Junctional epidermolysis bullosa</a></span><ul><li><span class="TLline"><a href="/medgen/1388385" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome">Epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/384018" ref="tree=MeSH" title="MedGen record for Epidermolysis Bullosa, Junctional, with Pyloric Atresia">Epidermolysis Bullosa, Junctional, with Pyloric Atresia</a></span></li><li><span class="TLline"><a href="/medgen/609458" ref="tree=MeSH" title="MedGen record for Generalized junctional epidermolysis bullosa non-Herlitz type">Generalized junctional epidermolysis bullosa non-Herlitz type</a></span></li><li><span class="TLline"><a href="/medgen/36328" ref="tree=MeSH" title="MedGen record for Junctional epidermolysis bullosa gravis of Herlitz">Junctional epidermolysis bullosa gravis of Herlitz</a></span></li><li><span class="TLline"><a href="/medgen/382142" ref="tree=MeSH" title="MedGen record for Junctional epidermolysis bullosa inversa">Junctional epidermolysis bullosa inversa</a></span></li><li><span class="TLline"><a href="/medgen/1810975" ref="tree=MeSH" title="MedGen record for Junctional epidermolysis bullosa with pyloric atresia">Junctional epidermolysis bullosa with pyloric atresia</a></span></li><li><span class="TLline"><a href="/medgen/82798" ref="tree=MeSH" title="MedGen record for Junctional epidermolysis bullosa, non-Herlitz type">Junctional epidermolysis bullosa, non-Herlitz type</a></span></li><li><span class="TLline"><a href="/medgen/272227" ref="tree=MeSH" title="MedGen record for Laryngo-onycho-cutaneous syndrome">Laryngo-onycho-cutaneous syndrome</a></span></li><li><span class="TLline"><a href="/medgen/930393" ref="tree=MeSH" title="MedGen record for Late-onset junctional epidermolysis bullosa">Late-onset junctional epidermolysis bullosa</a></span></li><li><span class="TLline"><a href="/medgen/341663" ref="tree=MeSH" title="MedGen record for Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome">Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1814511" ref="tree=MeSH" title="MedGen record for Localized junctional epidermolysis bullosa, non-Herlitz type">Localized junctional epidermolysis bullosa, non-Herlitz type</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/20779" ref="tree=MeSH" title="MedGen record for Genodermatosis">Genodermatosis</a></span><ul><li><span class="TLline"><a href="/medgen/182" ref="tree=MeSH" title="MedGen record for Albinism">Albinism</a></span><ul><li><span class="TLline"><a href="/medgen/3347" ref="tree=MeSH" title="MedGen record for Chédiak-Higashi syndrome">Chédiak-Higashi syndrome</a></span></li><li><span class="TLline"><a href="/medgen/38147" ref="tree=MeSH" title="MedGen record for Ocular albinism">Ocular albinism</a></span></li><li><span class="TLline"><a href="/medgen/90991" ref="tree=MeSH" title="MedGen record for Ocular albinism, type I">Ocular albinism, type I</a></span></li><li><span class="TLline"><a href="/medgen/36250" ref="tree=MeSH" title="MedGen record for Oculocutaneous albinism">Oculocutaneous albinism</a></span></li><li><span class="TLline"><a href="/medgen/36361" ref="tree=MeSH" title="MedGen record for Piebaldism">Piebaldism</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/41502" ref="tree=MeSH" title="MedGen record for Atopic eczema">Atopic eczema</a></span><ul><li><span class="TLline"><a href="/medgen/350353" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic">Dermatitis, atopic</a></span></li><li><span class="TLline"><a href="/medgen/340100" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic, 2">Dermatitis, atopic, 2</a></span></li><li><span class="TLline"><a href="/medgen/344173" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic, 3">Dermatitis, atopic, 3</a></span></li><li><span class="TLline"><a href="/medgen/340099" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic, 4">Dermatitis, atopic, 4</a></span></li><li><span class="TLline"><a href="/medgen/381292" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic, 5">Dermatitis, atopic, 5</a></span></li><li><span class="TLline"><a href="/medgen/344154" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic, 6">Dermatitis, atopic, 6</a></span></li><li><span class="TLline"><a href="/medgen/414058" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic, 7">Dermatitis, atopic, 7</a></span></li><li><span class="TLline"><a href="/medgen/462113" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic, 8">Dermatitis, atopic, 8</a></span></li><li><span class="TLline"><a href="/medgen/462114" ref="tree=MeSH" title="MedGen record for Dermatitis, atopic, 9">Dermatitis, atopic, 9</a></span></li><li><span class="TLline"><a href="/medgen/870398" ref="tree=MeSH" title="MedGen record for Late onset atopic dermatitis">Late onset atopic dermatitis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/108185" ref="tree=MeSH" title="MedGen record for Beaded hair">Beaded hair</a></span></li><li><span class="TLline"><a href="/medgen/86936" ref="tree=MeSH" title="MedGen record for Congenital ichthyosiform erythroderma">Congenital ichthyosiform erythroderma</a></span><ul><li><span class="TLline"><a href="/medgen/38180" ref="tree=MeSH" title="MedGen record for Congenital nonbullous ichthyosiform erythroderma">Congenital nonbullous ichthyosiform erythroderma</a></span></li><li><span class="TLline"><a href="/medgen/38179" ref="tree=MeSH" title="MedGen record for Epidermolytic ichthyosis">Epidermolytic ichthyosis</a></span></li><li><span class="TLline"><a href="/medgen/78578" ref="tree=MeSH" title="MedGen record for Ichthyosis linearis circumflexa">Ichthyosis linearis circumflexa</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/8206" ref="tree=MeSH" title="MedGen record for Cutis laxa">Cutis laxa</a></span><ul><li><span class="TLline"><a href="/medgen/347942" ref="tree=MeSH" title="MedGen record for Arterial tortuosity syndrome">Arterial tortuosity syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78663" ref="tree=MeSH" title="MedGen record for Autosomal recessive cutis laxa type 1">Autosomal recessive cutis laxa type 1</a></span></li><li><span class="TLline"><a href="/medgen/393947" ref="tree=MeSH" title="MedGen record for Craniofaciofrontodigital syndrome">Craniofaciofrontodigital syndrome</a></span></li><li><span class="TLline"><a href="/medgen/442566" ref="tree=MeSH" title="MedGen record for Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies">Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies</a></span></li><li><span class="TLline"><a href="/medgen/120630" ref="tree=MeSH" title="MedGen record for Cutis laxa, autosomal dominant">Cutis laxa, autosomal dominant</a></span></li><li><span class="TLline"><a href="/medgen/82793" ref="tree=MeSH" title="MedGen record for Cutis laxa, X-linked">Cutis laxa, X-linked</a></span></li><li><span class="TLline"><a href="/medgen/82794" ref="tree=MeSH" title="MedGen record for de Barsy syndrome">de Barsy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98149" ref="tree=MeSH" title="MedGen record for Geroderma osteodysplastica">Geroderma osteodysplastica</a></span></li><li><span class="TLline"><a href="/medgen/1673111" ref="tree=MeSH" title="MedGen record for Lethal arteriopathy syndrome due to fibulin-4 deficiency">Lethal arteriopathy syndrome due to fibulin-4 deficiency</a></span></li><li><span class="TLline"><a href="/medgen/154379" ref="tree=MeSH" title="MedGen record for Redundant skin">Redundant skin</a></span></li><li><span class="TLline"><a href="/medgen/416526" ref="tree=MeSH" title="MedGen record for RIN2 syndrome">RIN2 syndrome</a></span></li><li><span class="TLline"><a href="/medgen/326461" ref="tree=MeSH" title="MedGen record for SCARF syndrome">SCARF syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/75587" ref="tree=MeSH" title="MedGen record for Erythrokeratodermia variabilis">Erythrokeratodermia variabilis</a></span></li><li><span class="TLline"><a href="/medgen/102408" ref="tree=MeSH" title="MedGen record for Erythropoietic porphyria">Erythropoietic porphyria</a></span></li><li><span class="TLline"><a href="/medgen/43100" ref="tree=MeSH" title="MedGen record for Familial benign pemphigus">Familial benign pemphigus</a></span></li><li><span class="TLline"><a href="/medgen/58119" ref="tree=MeSH" title="MedGen record for Hepatic porphyria">Hepatic porphyria</a></span><ul><li><span class="TLline"><a href="/medgen/56452" ref="tree=MeSH" title="MedGen record for Acute intermittent porphyria">Acute intermittent porphyria</a></span></li><li><span class="TLline"><a href="/medgen/56455" ref="tree=MeSH" title="MedGen record for Erythropoietic protoporphyria">Erythropoietic protoporphyria</a></span></li><li><span class="TLline"><a href="/medgen/57940" ref="tree=MeSH" title="MedGen record for Hepatoerythropoietic porphyria">Hepatoerythropoietic porphyria</a></span></li><li><span class="TLline"><a href="/medgen/57931" ref="tree=MeSH" title="MedGen record for Hereditary coproporphyria">Hereditary coproporphyria</a></span></li><li><span class="TLline"><a href="/medgen/78659" ref="tree=MeSH" title="MedGen record for Porphobilinogen synthase deficiency">Porphobilinogen synthase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/56453" ref="tree=MeSH" title="MedGen record for Porphyria cutanea tarda">Porphyria cutanea tarda</a></span></li><li><span class="TLline"><a href="/medgen/58118" ref="tree=MeSH" title="MedGen record for Variegate porphyria">Variegate porphyria</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/199651" ref="tree=MeSH" title="MedGen record for Hereditary periodic fever syndrome">Hereditary periodic fever syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/934581" ref="tree=MeSH" title="MedGen record for Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive">Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive</a></span></li><li><span class="TLline"><a href="/medgen/2568" ref="tree=MeSH" title="MedGen record for Behcet disease">Behcet disease</a></span></li><li><span class="TLline"><a href="/medgen/1799987" ref="tree=MeSH" title="MedGen record for CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome">CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome</a></span></li><li><span class="TLline"><a href="/medgen/412215" ref="tree=MeSH" title="MedGen record for Cryopyrin associated periodic syndrome">Cryopyrin associated periodic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/87453" ref="tree=MeSH" title="MedGen record for Deficiency of mevalonate kinase">Deficiency of mevalonate kinase</a></span></li><li><span class="TLline"><a href="/medgen/435869" ref="tree=MeSH" title="MedGen record for Familial cold autoinflammatory syndrome 2">Familial cold autoinflammatory syndrome 2</a></span></li><li><span class="TLline"><a href="/medgen/863713" ref="tree=MeSH" title="MedGen record for Familial cold autoinflammatory syndrome 4">Familial cold autoinflammatory syndrome 4</a></span></li><li><span class="TLline"><a href="/medgen/45811" ref="tree=MeSH" title="MedGen record for Familial Mediterranean fever">Familial Mediterranean fever</a></span></li><li><span class="TLline"><a href="/medgen/863504" ref="tree=MeSH" title="MedGen record for Periodic fever-infantile enterocolitis-autoinflammatory syndrome">Periodic fever-infantile enterocolitis-autoinflammatory syndrome</a></span></li><li><span class="TLline"><a href="/medgen/226899" ref="tree=MeSH" title="MedGen record for TNF receptor-associated periodic fever syndrome (TRAPS)">TNF receptor-associated periodic fever syndrome (TRAPS)</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/7002" ref="tree=MeSH" title="MedGen record for Ichthyosis">Ichthyosis</a></span><ul><li><span class="TLline"><a href="/medgen/78092" ref="tree=MeSH" title="MedGen record for Acquired ichthyosis">Acquired ichthyosis</a></span></li><li><span class="TLline"><a href="/medgen/854762" ref="tree=MeSH" title="MedGen record for Autosomal recessive congenital ichthyosis 2">Autosomal recessive congenital ichthyosis 2</a></span></li><li><span class="TLline"><a href="/medgen/765442" ref="tree=MeSH" title="MedGen record for Generalized ichthyosis">Generalized ichthyosis</a></span></li><li><span class="TLline"><a href="/medgen/116092" ref="tree=MeSH" title="MedGen record for Harlequin fetus">Harlequin fetus</a></span></li><li><span class="TLline"><a href="/medgen/98153" ref="tree=MeSH" title="MedGen record for Ichthyosis bullosa of Siemens">Ichthyosis bullosa of Siemens</a></span></li><li><span class="TLline"><a href="/medgen/1615578" ref="tree=MeSH" title="MedGen record for Ichthyosis follicularis">Ichthyosis follicularis</a></span></li><li><span class="TLline"><a href="/medgen/38217" ref="tree=MeSH" title="MedGen record for Ichthyosis vulgaris">Ichthyosis vulgaris</a></span></li><li><span class="TLline"><a href="/medgen/354561" ref="tree=MeSH" title="MedGen record for Palmoplantar keratoderma, epidermolytic">Palmoplantar keratoderma, epidermolytic</a></span></li><li><span class="TLline"><a href="/medgen/867218" ref="tree=MeSH" title="MedGen record for Postnatal-onset ichthyosiform erythroderma">Postnatal-onset ichthyosiform erythroderma</a></span></li><li><span class="TLline"><a href="/medgen/11443" ref="tree=MeSH" title="MedGen record for Sjögren-Larsson syndrome">Sjögren-Larsson syndrome</a></span></li><li><span class="TLline"><a href="/medgen/86937" ref="tree=MeSH" title="MedGen record for X-linked ichthyosis with steryl-sulfatase deficiency">X-linked ichthyosis with steryl-sulfatase deficiency</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/411197" ref="tree=MeSH" title="MedGen record for Juvenile hyaline fibromatosis">Juvenile hyaline fibromatosis</a></span></li><li><span class="TLline"><a href="/medgen/5956" ref="tree=MeSH" title="MedGen record for Keratosis follicularis">Keratosis follicularis</a></span></li><li><span class="TLline"><a href="/medgen/6112" ref="tree=MeSH" title="MedGen record for Lipid proteinosis">Lipid proteinosis</a></span></li><li><span class="TLline"><a href="/medgen/231157" ref="tree=MeSH" title="MedGen record for Muir-Torré syndrome">Muir-Torré syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1635750" ref="tree=MeSH" title="MedGen record for Palmoplantar keratoderma">Palmoplantar keratoderma</a></span><ul><li><span class="TLline"><a href="/medgen/7201" ref="tree=MeSH" title="MedGen record for Diffuse palmoplantar hyperkeratosis">Diffuse palmoplantar hyperkeratosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/56518" ref="tree=MeSH" title="MedGen record for Porokeratosis">Porokeratosis</a></span><ul><li><span class="TLline"><a href="/medgen/120561" ref="tree=MeSH" title="MedGen record for Disseminated superficial actinic porokeratosis">Disseminated superficial actinic porokeratosis</a></span></li><li><span class="TLline"><a href="/medgen/56517" ref="tree=MeSH" title="MedGen record for Porokeratosis of Mantoux">Porokeratosis of Mantoux</a></span></li><li><span class="TLline"><a href="/medgen/181842" ref="tree=MeSH" title="MedGen record for Porokeratosis of Mibelli">Porokeratosis of Mibelli</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/120647" ref="tree=MeSH" title="MedGen record for Prolidase deficiency">Prolidase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/18733" ref="tree=MeSH" title="MedGen record for Pseudoxanthoma elasticum">Pseudoxanthoma elasticum</a></span><ul><li><span class="TLline"><a href="/medgen/698082" ref="tree=MeSH" title="MedGen record for Acquired pseudoxanthoma elasticum">Acquired pseudoxanthoma elasticum</a></span></li><li><span class="TLline"><a href="/medgen/698415" ref="tree=MeSH" title="MedGen record for Autosomal recessive inherited pseudoxanthoma elasticum">Autosomal recessive inherited pseudoxanthoma elasticum</a></span></li><li><span class="TLline"><a href="/medgen/697574" ref="tree=MeSH" title="MedGen record for Inherited pseudoxanthoma elasticum">Inherited pseudoxanthoma elasticum</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10819" ref="tree=MeSH" title="MedGen record for Rothmund-Thomson syndrome">Rothmund-Thomson syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/1684764" ref="tree=MeSH" title="MedGen record for Rothmund-Thomson syndrome type 1">Rothmund-Thomson syndrome type 1</a></span></li><li><span class="TLline"><a href="/medgen/1684753" ref="tree=MeSH" title="MedGen record for Rothmund-Thomson syndrome type 2">Rothmund-Thomson syndrome type 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/328433" ref="tree=MeSH" title="MedGen record for White sponge nevus">White sponge nevus</a></span></li><li><span class="TLline"><a href="/medgen/21943" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum">Xeroderma pigmentosum</a></span><ul><li><span class="TLline"><a href="/medgen/468518" ref="tree=MeSH" title="MedGen record for ERCC1-Related Xeroderma Pigmentosum">ERCC1-Related Xeroderma Pigmentosum</a></span></li><li><span class="TLline"><a href="/medgen/82775" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum group A">Xeroderma pigmentosum group A</a></span></li><li><span class="TLline"><a href="/medgen/78643" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum group B">Xeroderma pigmentosum group B</a></span></li><li><span class="TLline"><a href="/medgen/376352" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum variant type">Xeroderma pigmentosum variant type</a></span></li><li><span class="TLline"><a href="/medgen/416702" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum, group C">Xeroderma pigmentosum, group C</a></span></li><li><span class="TLline"><a href="/medgen/75656" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum, group D">Xeroderma pigmentosum, group D</a></span></li><li><span class="TLline"><a href="/medgen/341219" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum, group E">Xeroderma pigmentosum, group E</a></span></li><li><span class="TLline"><a href="/medgen/120612" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum, group F">Xeroderma pigmentosum, group F</a></span></li><li><span class="TLline"><a href="/medgen/75657" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum, group G">Xeroderma pigmentosum, group G</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/65911" ref="tree=MeSH" title="MedGen record for Nevus flammeus">Nevus flammeus</a></span><ul><li><span class="TLline"><a href="/medgen/340225" ref="tree=MeSH" title="MedGen record for Naevus flammeus of the eyelid">Naevus flammeus of the eyelid</a></span></li><li><span class="TLline"><a href="/medgen/870384" ref="tree=MeSH" title="MedGen record for Nevus flammeus nuchae">Nevus flammeus nuchae</a></span></li><li><span class="TLline"><a href="/medgen/376454" ref="tree=MeSH" title="MedGen record for Nevus flammeus of the forehead">Nevus flammeus of the forehead</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/20677" ref="tree=MeSH" title="MedGen record for Sclerema neonatorum">Sclerema neonatorum</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
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|
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<div class="portlet mgSection" id="ID_105">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
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<div class="nl"><a target="_blank" href="/pubmed/37166753">Keratosis pilaris: an update and approach to management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kodali N,
|
||
Patel VM,
|
||
Schwartz RA</span><br />
|
||
<span class="medgenPMjournal">Ital J Dermatol Venerol</span>
|
||
2023 Jun;158(3):217-223.
|
||
Epub 2023 May 11
|
||
doi: 10.23736/S2784-8671.23.07594-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37166753" target="_blank">37166753</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30584062">Clinical Practice Guideline for the Management of Infantile Hemangiomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krowchuk DP,
|
||
Frieden IJ,
|
||
Mancini AJ,
|
||
Darrow DH,
|
||
Blei F,
|
||
Greene AK,
|
||
Annam A,
|
||
Baker CN,
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||
Frommelt PC,
|
||
Hodak A,
|
||
Pate BM,
|
||
Pelletier JL,
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||
Sandrock D,
|
||
Weinberg ST,
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||
Whelan MA;
|
||
SUBCOMMITTEE ON THE MANAGEMENT OF INFANTILE HEMANGIOMAS</span><br />
|
||
<span class="medgenPMjournal">Pediatrics</span>
|
||
2019 Jan;143(1)
|
||
doi: 10.1542/peds.2018-3475.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30584062" target="_blank">30584062</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27659028">PHACE Syndrome: Consensus-Derived Diagnosis and Care Recommendations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Garzon MC,
|
||
Epstein LG,
|
||
Heyer GL,
|
||
Frommelt PC,
|
||
Orbach DB,
|
||
Baylis AL,
|
||
Blei F,
|
||
Burrows PE,
|
||
Chamlin SL,
|
||
Chun RH,
|
||
Hess CP,
|
||
Joachim S,
|
||
Johnson K,
|
||
Kim W,
|
||
Liang MG,
|
||
Maheshwari M,
|
||
McCoy GN,
|
||
Metry DW,
|
||
Monrad PA,
|
||
Pope E,
|
||
Powell J,
|
||
Shwayder TA,
|
||
Siegel DH,
|
||
Tollefson MM,
|
||
Vadivelu S,
|
||
Lew SM,
|
||
Frieden IJ,
|
||
Drolet BA</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2016 Nov;178:24-33.e2.
|
||
Epub 2016 Sep 19
|
||
doi: 10.1016/j.jpeds.2016.07.054.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27659028" target="_blank">27659028</a><a href="/pmc/articles/PMC6599593" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(congenital%20anomaly%20of%20skin)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (1580)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37143135">Pediatric joint hypermobility: a diagnostic framework and narrative review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tofts LJ,
|
||
Simmonds J,
|
||
Schwartz SB,
|
||
Richheimer RM,
|
||
O'Connor C,
|
||
Elias E,
|
||
Engelbert R,
|
||
Cleary K,
|
||
Tinkle BT,
|
||
Kline AD,
|
||
Hakim AJ,
|
||
van Rossum MAJ,
|
||
Pacey V</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2023 May 4;18(1):104.
|
||
doi: 10.1186/s13023-023-02717-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37143135" target="_blank">37143135</a><a href="/pmc/articles/PMC10157984" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34036913">Epidermolysis Bullosa: Pediatric Perspectives.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hon KL,
|
||
Chu S,
|
||
Leung AKC</span><br />
|
||
<span class="medgenPMjournal">Curr Pediatr Rev</span>
|
||
2022;18(3):182-190.
|
||
doi: 10.2174/1573396317666210525161252.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34036913" target="_blank">34036913</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34292508">Investigational Treatments for Epidermolysis Bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hou PC,
|
||
Wang HT,
|
||
Abhee S,
|
||
Tu WT,
|
||
McGrath JA,
|
||
Hsu CK</span><br />
|
||
<span class="medgenPMjournal">Am J Clin Dermatol</span>
|
||
2021 Nov;22(6):801-817.
|
||
Epub 2021 Jul 22
|
||
doi: 10.1007/s40257-021-00626-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34292508" target="_blank">34292508</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32973163">Epidermolysis bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bardhan A,
|
||
Bruckner-Tuderman L,
|
||
Chapple ILC,
|
||
Fine JD,
|
||
Harper N,
|
||
Has C,
|
||
Magin TM,
|
||
Marinkovich MP,
|
||
Marshall JF,
|
||
McGrath JA,
|
||
Mellerio JE,
|
||
Polson R,
|
||
Heagerty AH</span><br />
|
||
<span class="medgenPMjournal">Nat Rev Dis Primers</span>
|
||
2020 Sep 24;6(1):78.
|
||
doi: 10.1038/s41572-020-0210-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32973163" target="_blank">32973163</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26945532">Inherited ichthyosis: Non-syndromic forms.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Takeichi T,
|
||
Akiyama M</span><br />
|
||
<span class="medgenPMjournal">J Dermatol</span>
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2016 Mar;43(3):242-51.
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<span class="bold">PMID: </span><a href="/pubmed/26945532" target="_blank">26945532</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20anomaly%20of%20skin%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (10517)</a></div><h3 class="subhead">Diagnosis</h3>
|
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<div class="nl"><a target="_blank" href="/pubmed/37938840">Disseminated Monomorphic Pink Papules.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Rusiñol L,
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<span class="bold">PMID: </span><a href="/pubmed/37938840" target="_blank">37938840</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/37075188">Dome-Shaped Periorbital Papule.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Ewulu A,
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Cardis M</span><br />
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2023 Feb;111(2):91-100.
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<span class="bold">PMID: </span><a href="/pubmed/37075188" target="_blank">37075188</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32692048">Hemangioma-related syndromes.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Valdebran M,
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<span class="bold">PMID: </span><a href="/pubmed/32692048" target="_blank">32692048</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/25821090">Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type compared to other heritable connective tissue disorders.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Colombi M,
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<div class="nl"><a target="_blank" href="/pubmed/21364014">Sacral dimples.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Zywicke HA,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20anomaly%20of%20skin%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (15323)</a></div><h3 class="subhead">Therapy</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37929839">Acrodermatitis Enteropathica.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Zhao M,
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<span class="bold">PMID: </span><a href="/pubmed/37929839" target="_blank">37929839</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/35218370">Secukinumab responses vary across the spectrum of congenital ichthyosis in adults.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Lefferdink R,
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Rangel SM,
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Chima M,
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Ibler E,
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Epub 2022 Feb 26
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<div class="nl"><a target="_blank" href="/pubmed/36253866">Orthodontic and dentofacial orthopedic treatments in patients with ectodermal dysplasia: a systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Cerezo-Cayuelas M,
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Pérez-Silva A,
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Serna-Muñoz C,
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<div class="nl"><a target="_blank" href="/pubmed/34844973">Terlipressin-induced skin necrosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Jain G,
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<div class="nl"><a target="_blank" href="/pubmed/28306230">The evidence-based rationale for physical therapy treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Engelbert RH,
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Juul-Kristensen B,
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Pacey V,
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de Wandele I,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20anomaly%20of%20skin%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (6415)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/32973163">Epidermolysis bullosa.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Bardhan A,
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Bruckner-Tuderman L,
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Chapple ILC,
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Harper N,
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Has C,
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Magin TM,
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Marinkovich MP,
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Marshall JF,
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Mellerio JE,
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<span class="bold">PMID: </span><a href="/pubmed/32973163" target="_blank">32973163</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32973138">Epidermolysis bullosa.</a></div>
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<div class="portlet_content ln"><span class="medgenPMjournal">Nat Rev Dis Primers</span>
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<span class="bold">PMID: </span><a href="/pubmed/32973138" target="_blank">32973138</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/31094135">Yunis-Varon Syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Siddique AW,
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Ahmed Z,
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Haider A,
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Khalid H,
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<span class="medgenPMjournal">J Ayub Med Coll Abbottabad</span>
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<span class="bold">PMID: </span><a href="/pubmed/31094135" target="_blank">31094135</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/21364014">Sacral dimples.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Zywicke HA,
|
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Rozzelle CJ</span><br />
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<span class="medgenPMjournal">Pediatr Rev</span>
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2011 Mar;32(3):109-13; quiz 114, 151.
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doi: 10.1542/pir.32-3-109.
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<span class="bold">PMID: </span><a href="/pubmed/21364014" target="_blank">21364014</a></div>
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|
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<div class="nl"><a target="_blank" href="/pubmed/21413658">Harlequin ichthyosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Akhdari N,
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Ouladsiad M,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20anomaly%20of%20skin%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (5464)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37143135">Pediatric joint hypermobility: a diagnostic framework and narrative review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Tofts LJ,
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Simmonds J,
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Schwartz SB,
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Richheimer RM,
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O'Connor C,
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Elias E,
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Engelbert R,
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Cleary K,
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Tinkle BT,
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Kline AD,
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Hakim AJ,
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van Rossum MAJ,
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<span class="bold">PMID: </span><a href="/pubmed/37143135" target="_blank">37143135</a><a href="/pmc/articles/PMC10157984" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36658199">Ichthyosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Gutiérrez-Cerrajero C,
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Sprecher E,
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Paller AS,
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Akiyama M,
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Mazereeuw-Hautier J,
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<span class="medgenPMjournal">Nat Rev Dis Primers</span>
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<span class="bold">PMID: </span><a href="/pubmed/36658199" target="_blank">36658199</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34921679">Enhancement of stratum corneum lipid structure improves skin barrier function and protects against irritation in adults with dry, eczema-prone skin.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Danby SG,
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Andrew PV,
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Kay LJ,
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Pinnock A,
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Chittock J,
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Brown K,
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|
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|
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<div class="nl"><a target="_blank" href="/pubmed/34036913">Epidermolysis Bullosa: Pediatric Perspectives.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Hon KL,
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Chu S,
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Leung AKC</span><br />
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<span class="medgenPMjournal">Curr Pediatr Rev</span>
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2022;18(3):182-190.
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doi: 10.2174/1573396317666210525161252.
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<span class="bold">PMID: </span><a href="/pubmed/34036913" target="_blank">34036913</a></div>
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|
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<div class="nl"><a target="_blank" href="/pubmed/33738549">The Beighton Score as a measure of generalised joint hypermobility.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Malek S,
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Reinhold EJ,
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Pearce GS</span><br />
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<span class="medgenPMjournal">Rheumatol Int</span>
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Epub 2021 Mar 18
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<span class="bold">PMID: </span><a href="/pubmed/33738549" target="_blank">33738549</a><a href="/pmc/articles/PMC8390395" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20anomaly%20of%20skin%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (6960)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/35750466">Hypermobile Ehlers-Danlos syndrome and disorders of the gastrointestinal tract: What the gastroenterologist needs to know.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Thwaites PA,
|
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Gibson PR,
|
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Burgell RE</span><br />
|
||
<span class="medgenPMjournal">J Gastroenterol Hepatol</span>
|
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2022 Sep;37(9):1693-1709.
|
||
Epub 2022 Jul 20
|
||
doi: 10.1111/jgh.15927.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35750466" target="_blank">35750466</a><a href="/pmc/articles/PMC9544979" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35359921">A Systematic Review of the Progression of Cutaneous Lupus to Systemic Lupus Erythematosus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Curtiss P,
|
||
Walker AM,
|
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Chong BF</span><br />
|
||
<span class="medgenPMjournal">Front Immunol</span>
|
||
2022;13:866319.
|
||
Epub 2022 Mar 11
|
||
doi: 10.3389/fimmu.2022.866319.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35359921" target="_blank">35359921</a><a href="/pmc/articles/PMC8963103" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32886029">Treatment of keratosis pilaris and its variants: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Maghfour J,
|
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Ly S,
|
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Haidari W,
|
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Taylor SL,
|
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Feldman SR</span><br />
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<span class="medgenPMjournal">J Dermatolog Treat</span>
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2022 May;33(3):1231-1242.
|
||
Epub 2020 Sep 14
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||
doi: 10.1080/09546634.2020.1818678.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32886029" target="_blank">32886029</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34145717">Physical therapy treatment of hypermobile Ehlers-Danlos syndrome: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Reychler G,
|
||
De Backer MM,
|
||
Piraux E,
|
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Poncin W,
|
||
Caty G</span><br />
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<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2021 Oct;185(10):2986-2994.
|
||
Epub 2021 Jun 19
|
||
doi: 10.1002/ajmg.a.62393.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34145717" target="_blank">34145717</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32668290">Rhupus: a systematic literature review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Antonini L,
|
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Le Mauff B,
|
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Marcelli C,
|
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Aouba A,
|
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de Boysson H</span><br />
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<span class="medgenPMjournal">Autoimmun Rev</span>
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2020 Sep;19(9):102612.
|
||
Epub 2020 Jul 12
|
||
doi: 10.1016/j.autrev.2020.102612.
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||
<span class="bold">PMID: </span><a href="/pubmed/32668290" target="_blank">32668290</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20anomaly%20of%20skin%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (226)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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