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<meta name="keywords" content="C0079683, bullosa letali, epidermolysis, bullosa letalis, epidermolysis, bullosa, herlitz-pearson-type epidermolysis, disease or syndrome, disease, herlitz, disease, herlitz's, epidermolysis bullosa hereditaria letalis, epidermolysis bullosa junctionalis, herlitz type, epidermolysis bullosa letali, epidermolysis bullosa letalis, epidermolysis bullosa, herlitz-pearson-type, epidermolysis bullosa, junctional 1b, severe, epidermolysis bullosa, junctional herlitz-pearson type, epidermolysis bullosa, junctional, generalized severe, epidermolysis bullosa, junctional, herlitz type, epidermolysis bullosa, junctional, herlitz-pearson type, herlitz disease, herlitz pearson type epidermolysis bullosa, herlitz syndrome, herlitz type epidermolysis bullosa junctionalis, herlitz's disease, herlitz-pearson type epidermolysis bullosa, herlitz-pearson-type epidermolysis bullosa, herlitz-type junctional epidermolysis bullosa, herlitzs disease, jeb, generalised severe, jeb, generalized severe, jeb-h, jeb-herlitz type, jeb1b, junctional epidermolysis bullosa generalisata gravis, junctional epidermolysis bullosa gravis of herlitz, junctional epidermolysis bullosa herlitz type, junctional epidermolysis bullosa, generalised severe, junctional epidermolysis bullosa, generalized severe, junctional epidermolysis bullosa, herlitz type, junctional epidermolysis bullosa, herlitz-pearson type, junctional epidermolysis bullosa, lethal type, herlitz, lama3, lamb3, lamc2, letali, epidermolysis bullosa, letalis, epidermolysis bullosa, lethal junctional epidermolysis bullosa, severe generalized jeb, severe generalized junctional epidermolysis bullosa, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="Junctional epidermolysis bullosa (JEB) is characterized by fragility of the skin and mucous membranes, manifest by blistering with little or no trauma. Blistering may be severe and granulation tissue can form on the skin around the oral and nasal cavities, fingers and toes, and internally around the upper airway. Blisters generally heal with no significant scarring. Broad classification of JEB includes JEB generalized severe and JEB generalized intermediate. In JEB generalized severe, blisters are present at birth or become apparent in the neonatal period. Congenital malformations of the urinary tract and bladder may also occur. In JEB generalized intermediate, the phenotype may be mild with blistering localized to hands, feet, knees, and elbows with or without renal or ureteral involvement. Some individuals never blister after the newborn period. Additional features shared by JEB and the other major forms of epidermolysis bullosa (EB) include congenital localized absence of skin (aplasia cutis congenita), milia, nail dystrophy, scarring alopecia, hypotrichosis, pseudosyndactyly, and other contractures." /><meta name="robots" content="index,nofollow,noarchive" />
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<div><div class="rprt full-rprt"><div class="portlet" style="border-top-style: none; margin-top: 0px; padding-top: 0px; margin-bottom: 0px; padding-left: 0.2em;">
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<!--
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||
UID=36328
|
||
ConceptID=C0079683
|
||
-->
|
||
<!--imgCountBooks = 2--><div class="ncbi_carousel" data-ncbicarousel-config="imageWidth:'100px',numItemsVisible:2,toggler:false"><div class="nc_header"><span class="img_strip_title">Images (2)</span></div><div class="nc_content"><div class="nc_item"><a class="figpopup"><img alt="Image from GeneReviews" src="/books/NBK1125/bin/ebj-Image002.gif" src-large="/books/NBK1125/bin/ebj-Image002.jpg" /></a><br /><a href="/books/NBK1125/figure/ebj.F2/" title="GeneReviews" target="_blank">details</a></div><div class="nc_item"><a class="figpopup"><img alt="Image from GeneReviews" src="/books/NBK1125/bin/ebj-Image001.gif" src-large="/books/NBK1125/bin/ebj-Image001.jpg" /></a><br /><a href="/books/NBK1125/figure/ebj.F1/" title="GeneReviews" target="_blank">details</a></div></div></div><h1 class="medgenTitle"><div class="MedGenTitleText">Junctional epidermolysis bullosa gravis of Herlitz<span class="h1sub">(JEB1B)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>36328</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.">C0079683</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>EPIDERMOLYSIS BULLOSA JUNCTIONALIS, HERLITZ TYPE; Epidermolysis Bullosa Letalis; EPIDERMOLYSIS BULLOSA, JUNCTIONAL 1B, SEVERE; EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ-PEARSON TYPE; Herlitz-Pearson type epidermolysis bullosa; Herlitz-type junctional epidermolysis bullosa; JEB-HERLITZ TYPE</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Epidermolysis bullosa, junctional Herlitz-Pearson type (79855003); Epidermolysis bullosa hereditaria letalis (79855003); Junctional epidermolysis bullosa gravis of Herlitz (400140006); Epidermolysis bullosa letalis (400140006); Junctional epidermolysis bullosa, lethal type, Herlitz (400140006); Herlitz syndrome (400140006); Herlitz's disease (400140006)</td></tr>
|
||
<tr><td>Modes of inheritance:</td>
|
||
<td>
|
||
<div class="divPopper rprt" id="moi_141025"><div><strong>Autosomal recessive inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141025</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.">C0441748</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Intellectual Product</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).</div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_141025" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive inheritance</a><span> (Orphanet)</span></div></td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Genes (locations):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
|
||
Gene(s) directly associated with<br />
|
||
this condition or phenotype.</div></td>
|
||
<td><a target="_blank" title="LAMA3 - ID: 3909 - NCBI Gene" href="/gene/3909" class="medgenPMinfo">LAMA3</a> (18q11.2); <a target="_blank" title="LAMB3 - ID: 3914 - NCBI Gene" href="/gene/3914" class="medgenPMinfo">LAMB3</a> (1q32.2); <a target="_blank" title="LAMC2 - ID: 3918 - NCBI Gene" href="/gene/3918" class="medgenPMinfo">LAMC2</a> (1q25.3)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0009182" target="_blank">MONDO:0009182</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/226700" target="_blank">226700</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=79404">ORPHA79404</a></td></tr></tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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||
<div class="portlet mgSection" id="ID_101">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Disease_characteristics">Disease characteristics</h1><a sid="101" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><div class="excerpt">Excerpted from the <i>GeneReview: </i><a href="/books/NBK1125" target="_blank">Junctional Epidermolysis Bullosa</a></div><div>Junctional epidermolysis bullosa (JEB) is characterized by fragility of the skin and mucous membranes, manifest by blistering with little or no trauma. Blistering may be severe and granulation tissue can form on the skin around the oral and nasal cavities, fingers and toes, and internally around the upper airway. Blisters generally heal with no significant scarring. Broad classification of JEB includes JEB generalized severe and JEB generalized intermediate. In JEB generalized severe, blisters are present at birth or become apparent in the neonatal period. Congenital malformations of the urinary tract and bladder may also occur. In JEB generalized intermediate, the phenotype may be mild with blistering localized to hands, feet, knees, and elbows with or without renal or ureteral involvement. Some individuals never blister after the newborn period. Additional features shared by JEB and the other major forms of epidermolysis bullosa (EB) include congenital localized absence of skin (aplasia cutis congenita), milia, nail dystrophy, scarring alopecia, hypotrichosis, pseudosyndactyly, and other contractures. [from <a title="GeneReviews" href="https://www.ncbi.nlm.nih.gov/books/NBK1116" class="defSource" target="_blank">GeneReviews</a>]</div><div class="spaceAbove"><strong>Full text of <i>GeneReview</i> (by section):</strong><br /><a class="medgenPMinfo" href="/books/NBK1125#ebj.Summary" target="NBK1125">Summary</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Diagnosis" target="NBK1125">Diagnosis</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Clinical_Characteristics" target="NBK1125">Clinical Characteristics</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Genetically_Related_Allelic_Disorder" target="NBK1125">Genetically Related (Allelic) Disorders</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Differential_Diagnosis" target="NBK1125">Differential Diagnosis</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Management" target="NBK1125">Management</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Genetic_Counseling" target="NBK1125">Genetic Counseling</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Resources" target="NBK1125">Resources</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Molecular_Genetics" target="NBK1125">Molecular Genetics</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.References" target="NBK1125">References</a> | <a class="medgenPMinfo" href="/books/NBK1125#ebj.Chapter_Notes" target="NBK1125">Chapter Notes</a></div><div class="spaceAbove"><strong>Authors:</strong><br />
|
||
Ellen G Pfendner | Anne W Lucky <a href="/books/NBK1125" target="NBK1125" title="NCBI Bookshelf: Junctional Epidermolysis Bullosa">view full author information</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_117">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Additional_descriptions">Additional descriptions</h1><a sid="117" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><div class="mgSection"><strong>From OMIM</strong><br />Severe junctional epidermolysis bullosa 1B (JEB1B) is an autosomal recessive skin blistering disorder characterized by extreme fragility of the skin and epithelia of various extracutaneous tissues. Blisters and erosions are present at birth. Blister formation occurs within the dermal-epidermal basement membrane zone. Patients usually die before 1 year of age (summary by Takizawa et al., 1998).
|
||
For a discussion of genetic heterogeneity of the subtypes of JEB, see JEB1A (226650).
|
||
Reviews
|
||
Pulkkinen and Uitto (1999) reviewed the pathophysiology and phenotypic and genetic heterogeneity of the various forms of epidermolysis bullosa. <a target="_blank" href="http://www.omim.org/entry/226700">http://www.omim.org/entry/226700</a></div><div class="mgSection"><strong>From MedlinePlus Genetics</strong><br />The milder form of junctional epidermolysis bullosa is called JEB generalized intermediate. The blistering associated with JEB generalized intermediate may be limited to the hands, feet, knees, and elbows, and it often improves after the newborn period. Other characteristic features of this form of the condition include hair loss, abnormal fingernails and toenails, and irregular tooth enamel. Most affected individuals do not have extensive scarring or granulation tissue formation, so breathing difficulties and other severe complications are rare. JEB generalized intermediate is typically associated with a normal lifespan.<br /><br />JEB generalized severe is the more serious form of the condition. From birth or early infancy, affected individuals have blistering over large regions of the body. Blistering also affects the mucous membranes, such as the moist lining of the mouth and digestive tract, which can make it difficult to eat and digest food. As a result, many affected children are undernourished and grow slowly. The extensive blistering leads to scarring and the formation of red, bumpy patches called granulation tissue. Granulation tissue bleeds easily and profusely, making affected infants susceptible to serious infections and loss of necessary proteins, minerals, and fluids. Additionally, a buildup of granulation tissue in the airway can lead to a weak, hoarse cry and difficulty breathing.<br /><br />Other complications of JEB generalized severe can include fusion of the fingers and toes, abnormalities of the fingernails and toenails, joint deformities (contractures) that limit movement, hair loss (alopecia), and thinning of the protective outer layer (enamel) of the teeth. Because the signs and symptoms of JEB generalized severe are so serious, infants with this condition usually do not survive beyond the first year of life.<br /><br />Junctional epidermolysis bullosa (JEB) is a major form of epidermolysis bullosa, a group of genetic conditions that cause the skin to be very fragile and to blister easily. Blisters and areas of skin loss (erosions) form in response to minor injury or friction, such as rubbing or scratching. Researchers classify junctional epidermolysis bullosa into two main types: JEB generalized severe (formerly known as Herlitz JEB) and JEB generalized intermediate (formerly known as non-Herlitz JEB). Although the types differ in severity, their features overlap significantly, and they can be caused by mutations in the same genes. <a target="_blank" href="https://medlineplus.gov/genetics/condition/junctional-epidermolysis-bullosa">https://medlineplus.gov/genetics/condition/junctional-epidermolysis-bullosa</a></div></div>
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||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_102">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
|
||
<div class="divPopper rprt" id="clin_52619"><div><strong>Syndactyly</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>52619</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.">C0039075</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
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||
<div class="spaceAbove">Webbing or fusion of the fingers or toes, involving soft parts only or including bone structure. Bony fusions are referred to as "bony" syndactyly if the fusion occurs in a radio-ulnar axis. Fusions of bones of the fingers or toes in a proximo-distal axis are referred to as "symphalangism".</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/52619">Feature record</a> | <a href="/medgen?term=%22Syndactyly%22%5BClinical%20Features%5D%20OR%2052619%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_746019"><div><strong>Failure to thrive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>746019</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.">C2315100</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/746019">Feature record</a> | <a href="/medgen?term=%22Failure%20to%20thrive%22%5BClinical%20Features%5D%20OR%20746019%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_196010"><div><strong>Congenital hypertrophic pyloric stenosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>196010</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.">C0700639</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Pyloric stenosis, also known as infantile hypertrophic pyloric stenosis, is an uncommon condition in infants characterized by abnormal thickening of the pylorus muscles in the stomach leading to gastric outlet obstruction. Clinically infants are well at birth. Then, at 3 to 6 weeks of age, the infants present with projectile vomiting, potentially leading to dehydration and weight loss.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/196010">Feature record</a> | <a href="/medgen?term=%22Congenital%20hypertrophic%20pyloric%20stenosis%22%5BClinical%20Features%5D%20OR%20196010%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_8288"><div><strong>Carious teeth</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>8288</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.">C0011334</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Caries is a multifactorial bacterial infection affecting the structure of the tooth. This term has been used to describe the presence of more than expected dental caries.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/8288">Feature record</a> | <a href="/medgen?term=%22Carious%20teeth%22%5BClinical%20Features%5D%20OR%208288%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_3730"><div><strong>Enamel hypoplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>3730</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.">C0011351</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Developmental hypoplasia of the dental enamel.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/3730">Feature record</a> | <a href="/medgen?term=%22Enamel%20hypoplasia%22%5BClinical%20Features%5D%20OR%203730%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_57875"><div><strong>Atrophic scars</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>57875</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.">C0162154</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Scars that form a depression compared to the level of the surrounding skin because of damage to the collagen, fat or other tissues below the skin.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/57875">Feature record</a> | <a href="/medgen?term=%22Atrophic%20scars%22%5BClinical%20Features%5D%20OR%2057875%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_66368"><div><strong>Nail dystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>66368</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.">C0221260</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Onychodystrophy (nail dystrophy) refers to nail changes apart from changes of the color (nail dyschromia) and involves partial or complete disruption of the various keratinous layers of the nail plate.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/66368">Feature record</a> | <a href="/medgen?term=%22Nail%20dystrophy%22%5BClinical%20Features%5D%20OR%2066368%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_87528"><div><strong>Milia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>87528</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.">C0345996</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Presence of multiple small cysts containing keratin (skin protein) and presenting as tiny pearly-white bumps just under the surface of the skin.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/87528">Feature record</a> | <a href="/medgen?term=%22Milia%22%5BClinical%20Features%5D%20OR%2087528%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_331737"><div><strong>Nail dysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>331737</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.">C1834405</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The presence of developmental dysplasia of the nail.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/331737">Feature record</a> | <a href="/medgen?term=%22Nail%20dysplasia%22%5BClinical%20Features%5D%20OR%20331737%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_412159"><div><strong>Abnormal blistering of the skin</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>412159</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.">C2132198</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The presence of one or more bullae on the skin, defined as fluid-filled blisters more than 5 mm in diameter with thin walls.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/412159">Feature record</a> | <a href="/medgen?term=%22Abnormal%20blistering%20of%20the%20skin%22%5BClinical%20Features%5D%20OR%20412159%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_388677"><div><strong>Congenital localized absence of skin</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>388677</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.">C2673597</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/388677">Feature record</a> | <a href="/medgen?term=%22Congenital%20localized%20absence%20of%20skin%22%5BClinical%20Features%5D%20OR%20388677%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_867365"><div><strong>Lamina lucida cleavage</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>867365</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.">C4021730</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The formation of bullae (blisters) with cleavage in the lamina lucida layer of the skin.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/867365">Feature record</a> | <a href="/medgen?term=%22Lamina%20lucida%20cleavage%22%5BClinical%20Features%5D%20OR%20867365%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite" data-jigconfig="closed: 1"><div class="concept-def"><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().openAll(); return false;">Show all</a><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().closeAll(); return false;">Hide all</a></div><ul><li><span class="TLline">Abnormality of head or neck</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_8288" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Carious teeth</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_3730" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Enamel hypoplasia</a></span></li></ul></li><li><span class="TLline">Abnormality of limbs</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_52619" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Syndactyly</a></span></li></ul></li><li><span class="TLline">Abnormality of the digestive system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_196010" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital hypertrophic pyloric stenosis</a></span></li></ul></li><li><span class="TLline">Abnormality of the integument</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_412159" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Abnormal blistering of the skin</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_57875" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Atrophic scars</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_388677" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital localized absence of skin</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_867365" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lamina lucida cleavage</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_87528" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Milia</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_331737" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nail dysplasia</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_66368" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nail dystrophy</a></span></li></ul></li><li><span class="TLline">Growth abnormality</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_746019" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Failure to thrive</a></span></li></ul></li></ul></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_118">
|
||
<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>
|
||
<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><li><a href="#tabORDO">Orphanet</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="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0079301[DISCUI]&test_type=Clinical" ref="ncbi_uid=86898">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=86898" target="_blank" href="/omim/226650">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1125/" ref="ncbi_uid=86898">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=86898" ref="ncbi_uid=86898">V</a></span></span><span class="TLline"><a href="/medgen/86898" ref="tree=GTR&ncbi_uid=86898&link_uid=86898" title="View MedGen record for 'Junctional epidermolysis bullosa'">Junctional epidermolysis bullosa</a></span><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0079683[DISCUI]&test_type=Clinical" ref="ncbi_uid=36328">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=36328" target="_blank" href="/omim/150310">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1125/" ref="ncbi_uid=36328">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=36328" ref="ncbi_uid=36328">V</a></span></span><span class="TLline">Junctional epidermolysis bullosa gravis of Herlitz</span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0268374[DISCUI]&test_type=Clinical" ref="ncbi_uid=82798">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=82798" target="_blank" href="/omim/150310">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/?term=(NBK1125%20OR%20NBK1304)%20AND%20gene%5Bbook%5D&showtype=onebook" ref="ncbi_uid=82798">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=82798" ref="ncbi_uid=82798">V</a></span></span><span class="TLline"><a href="/medgen/82798" ref="tree=GTR&ncbi_uid=82798&link_uid=82798" title="View MedGen record for 'Junctional epidermolysis bullosa, non-Herlitz type'">Junctional epidermolysis bullosa, non-Herlitz type</a></span></li></ul></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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="TLline"><a href="/medgen/11449" ref="tree=MeSH" title="MedGen record for Congenital anomaly of skin">Congenital anomaly of skin</a></span><ul><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/86898" ref="tree=MeSH" title="MedGen record for Junctional epidermolysis bullosa">Junctional epidermolysis bullosa</a></span><ul><li><span class="matched_ds">Junctional epidermolysis bullosa gravis of Herlitz</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div><div id="tabORDO">Follow <a target="_blank" href="http://www.orpha.net/consor/cgi-bin/Disease_Classif.php?lng=EN&data_id=156&PatId=11430&search=Disease_Classif_Simple&new=1" class="ital bold">this link</a> to review classifications for <span class="ital">Junctional epidermolysis bullosa gravis of Herlitz</span> in Orphanet.</div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<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>
|
||
<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>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36287101">Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen F,
|
||
Wei R,
|
||
Deng D,
|
||
Zhang X,
|
||
Cao Y,
|
||
Pan C,
|
||
Wang Y,
|
||
Cao Q,
|
||
Wang J,
|
||
Zeng M,
|
||
Huang L,
|
||
Gu Y,
|
||
Yao Z,
|
||
Li M</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2023 Feb;37(2):411-419.
|
||
Epub 2022 Nov 5
|
||
doi: 10.1111/jdv.18692.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36287101" target="_blank">36287101</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33202040">Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krämer S,
|
||
Lucas J,
|
||
Gamboa F,
|
||
Peñarrocha Diago M,
|
||
Peñarrocha Oltra D,
|
||
Guzmán-Letelier M,
|
||
Paul S,
|
||
Molina G,
|
||
Sepúlveda L,
|
||
Araya I,
|
||
Soto R,
|
||
Arriagada C,
|
||
Lucky AW,
|
||
Mellerio JE,
|
||
Cornwall R,
|
||
Alsayer F,
|
||
Schilke R,
|
||
Antal MA,
|
||
Castrillón F,
|
||
Paredes C,
|
||
Serrano MC,
|
||
Clark V</span><br />
|
||
<span class="medgenPMjournal">Spec Care Dentist</span>
|
||
2020 Nov;40 Suppl 1(Suppl 1):3-81.
|
||
doi: 10.1111/scd.12511.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33202040" target="_blank">33202040</a><a href="/pmc/articles/PMC7756753" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12677429">Japanese guidelines for diagnosis and treatment of junctional and dystrophic epidermolysis bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tamai K,
|
||
Hashimoto I,
|
||
Hanada K,
|
||
Ikeda S,
|
||
Imamura S,
|
||
Ogawa H;
|
||
Japanese Study Group for Rare Intractable Skin Diseases</span><br />
|
||
<span class="medgenPMjournal">Arch Dermatol Res</span>
|
||
2003 Apr;295 Suppl 1:S24-8.
|
||
Epub 2003 Mar 11
|
||
doi: 10.1007/s00403-002-0379-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12677429" target="_blank">12677429</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(junctional%20epidermolysis%20bullosa%20gravis%20of%20herlitz)%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 (41)</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/36287101">Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen F,
|
||
Wei R,
|
||
Deng D,
|
||
Zhang X,
|
||
Cao Y,
|
||
Pan C,
|
||
Wang Y,
|
||
Cao Q,
|
||
Wang J,
|
||
Zeng M,
|
||
Huang L,
|
||
Gu Y,
|
||
Yao Z,
|
||
Li M</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2023 Feb;37(2):411-419.
|
||
Epub 2022 Nov 5
|
||
doi: 10.1111/jdv.18692.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36287101" target="_blank">36287101</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/32732072">Inherited epidermolysis bullosa: update on the clinical and genetic aspects.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mariath LM,
|
||
Santin JT,
|
||
Schuler-Faccini L,
|
||
Kiszewski AE</span><br />
|
||
<span class="medgenPMjournal">An Bras Dermatol</span>
|
||
2020 Sep-Oct;95(5):551-569.
|
||
Epub 2020 Jul 8
|
||
doi: 10.1016/j.abd.2020.05.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32732072" target="_blank">32732072</a><a href="/pmc/articles/PMC7563003" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Junctional%20epidermolysis%20bullosa%20gravis%20of%20Herlitz%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 (234)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36287101">Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen F,
|
||
Wei R,
|
||
Deng D,
|
||
Zhang X,
|
||
Cao Y,
|
||
Pan C,
|
||
Wang Y,
|
||
Cao Q,
|
||
Wang J,
|
||
Zeng M,
|
||
Huang L,
|
||
Gu Y,
|
||
Yao Z,
|
||
Li M</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2023 Feb;37(2):411-419.
|
||
Epub 2022 Nov 5
|
||
doi: 10.1111/jdv.18692.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36287101" target="_blank">36287101</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/32732072">Inherited epidermolysis bullosa: update on the clinical and genetic aspects.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mariath LM,
|
||
Santin JT,
|
||
Schuler-Faccini L,
|
||
Kiszewski AE</span><br />
|
||
<span class="medgenPMjournal">An Bras Dermatol</span>
|
||
2020 Sep-Oct;95(5):551-569.
|
||
Epub 2020 Jul 8
|
||
doi: 10.1016/j.abd.2020.05.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32732072" target="_blank">32732072</a><a href="/pmc/articles/PMC7563003" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Junctional%20epidermolysis%20bullosa%20gravis%20of%20Herlitz%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 (277)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36730504">Sucralfate-based cream as a novel and cost-effective topical agent in poorly healing ulcers in junctional epidermolysis bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agrawal A,
|
||
Bhardwaj A</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Dermatol</span>
|
||
2023 Feb 2;48(2):138-140.
|
||
doi: 10.1093/ced/llac048.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36730504" target="_blank">36730504</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36689495">Efficacy and safety of Oleogel-S10 (birch triterpenes) for epidermolysis bullosa: results from the phase III randomized double-blind phase of the EASE study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kern JS,
|
||
Sprecher E,
|
||
Fernandez MF,
|
||
Schauer F,
|
||
Bodemer C,
|
||
Cunningham T,
|
||
Löwe S,
|
||
Davis C,
|
||
Sumeray M,
|
||
Bruckner AL,
|
||
Murrell DF;
|
||
EASE investigators</span><br />
|
||
<span class="medgenPMjournal">Br J Dermatol</span>
|
||
2023 Jan 23;188(1):12-21.
|
||
doi: 10.1093/bjd/ljac001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36689495" target="_blank">36689495</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31068252">Gene Therapy for Epidermolysis Bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marinkovich MP,
|
||
Tang JY</span><br />
|
||
<span class="medgenPMjournal">J Invest Dermatol</span>
|
||
2019 Jun;139(6):1221-1226.
|
||
Epub 2019 May 5
|
||
doi: 10.1016/j.jid.2018.11.036.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31068252" target="_blank">31068252</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30395395">Bullous autoimmune dermatoses.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hofmann SC,
|
||
Juratli HA,
|
||
Eming R</span><br />
|
||
<span class="medgenPMjournal">J Dtsch Dermatol Ges</span>
|
||
2018 Nov;16(11):1339-1358.
|
||
doi: 10.1111/ddg.13688.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30395395" target="_blank">30395395</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27846969">Topical timolol for chronic wounds in patients with junctional epidermolysis bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chiaverini C,
|
||
Passeron T,
|
||
Lacour JP</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2016 Dec;75(6):e223-e224.
|
||
doi: 10.1016/j.jaad.2016.08.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27846969" target="_blank">27846969</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Junctional%20epidermolysis%20bullosa%20gravis%20of%20Herlitz%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 (72)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<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/32973163">Epidermolysis bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bardhan A,
|
||
Bruckner-Tuderman L,
|
||
Chapple ILC,
|
||
Fine JD,
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Has C,
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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/32686866">Epidermolysis bullosa with congenital absence of skin: Review of the literature.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Martinez-Moreno A,
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<div class="nl"><a target="_blank" href="/pubmed/19945620">Laryngo-onycho-cutaneous syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Cohn HI,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Junctional%20epidermolysis%20bullosa%20gravis%20of%20Herlitz%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 (170)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/38157931">Genotype-Phenotype Correlation in Junctional Epidermolysis Bullosa: Signposts to Severity.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wen D,
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Hunjan M,
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2024 Jun;144(6):1334-1343.e14.
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Epub 2023 Dec 28
|
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doi: 10.1016/j.jid.2023.11.021.
|
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<span class="bold">PMID: </span><a href="/pubmed/38157931" target="_blank">38157931</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/37638011">Autoimmunity against laminin 332.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Patzelt S,
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Schmidt E</span><br />
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<span class="medgenPMjournal">Front Immunol</span>
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Epub 2023 Aug 10
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doi: 10.3389/fimmu.2023.1250115.
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<span class="bold">PMID: </span><a href="/pubmed/37638011" target="_blank">37638011</a><a href="/pmc/articles/PMC10449457" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/36287101">Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Chen F,
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Wei R,
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Deng D,
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Zhang X,
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Cao Y,
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Pan C,
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Wang Y,
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Cao Q,
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Wang J,
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Zeng M,
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Huang L,
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Gu Y,
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Yao Z,
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Li M</span><br />
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<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
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2023 Feb;37(2):411-419.
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Epub 2022 Nov 5
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doi: 10.1111/jdv.18692.
|
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<span class="bold">PMID: </span><a href="/pubmed/36287101" target="_blank">36287101</a></div>
|
||
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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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||
<div class="nl"><a target="_blank" href="/pubmed/32246433">Quality of life in people with epidermolysis bullosa: a systematic review.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Togo CCG,
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Zidorio APC,
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Gonçalves VSS,
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Hubbard L,
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de Carvalho KMB,
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Dutra ES</span><br />
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<span class="medgenPMjournal">Qual Life Res</span>
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2020 Jul;29(7):1731-1745.
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Epub 2020 Apr 3
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doi: 10.1007/s11136-020-02495-5.
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||
<span class="bold">PMID: </span><a href="/pubmed/32246433" target="_blank">32246433</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Junctional%20epidermolysis%20bullosa%20gravis%20of%20Herlitz%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 (154)</a></div></div>
|
||
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|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
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<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/38096448">Oral Prosthetic Rehabilitation in Patients with Epidermolysis Bullosa Hereditaria: A Systematic Review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mascarell S,
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Citterio H,
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Le Roux É,
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Berdal A,
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Lescaille G,
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Friedlander L</span><br />
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<span class="medgenPMjournal">Int J Prosthodont</span>
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||
2024 Nov 22;37(6):699-710.
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doi: 10.11607/ijp.8791.
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||
<span class="bold">PMID: </span><a href="/pubmed/38096448" target="_blank">38096448</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33202040">Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krämer S,
|
||
Lucas J,
|
||
Gamboa F,
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Peñarrocha Diago M,
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Peñarrocha Oltra D,
|
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Guzmán-Letelier M,
|
||
Paul S,
|
||
Molina G,
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||
Sepúlveda L,
|
||
Araya I,
|
||
Soto R,
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Arriagada C,
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Lucky AW,
|
||
Mellerio JE,
|
||
Cornwall R,
|
||
Alsayer F,
|
||
Schilke R,
|
||
Antal MA,
|
||
Castrillón F,
|
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Paredes C,
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||
Serrano MC,
|
||
Clark V</span><br />
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||
<span class="medgenPMjournal">Spec Care Dentist</span>
|
||
2020 Nov;40 Suppl 1(Suppl 1):3-81.
|
||
doi: 10.1111/scd.12511.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33202040" target="_blank">33202040</a><a href="/pmc/articles/PMC7756753" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32246433">Quality of life in people with epidermolysis bullosa: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Togo CCG,
|
||
Zidorio APC,
|
||
Gonçalves VSS,
|
||
Hubbard L,
|
||
de Carvalho KMB,
|
||
Dutra ES</span><br />
|
||
<span class="medgenPMjournal">Qual Life Res</span>
|
||
2020 Jul;29(7):1731-1745.
|
||
Epub 2020 Apr 3
|
||
doi: 10.1007/s11136-020-02495-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32246433" target="_blank">32246433</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29935895">Clinical outcomes and molecular profile of patients with Carmi syndrome: A systematic review and evidence quality assessment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mylonas KS,
|
||
Hayes M,
|
||
Ko LN,
|
||
Griggs CL,
|
||
Kroshinsky D,
|
||
Masiakos PT</span><br />
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<span class="medgenPMjournal">J Pediatr Surg</span>
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||
2019 Jul;54(7):1351-1358.
|
||
Epub 2018 May 29
|
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doi: 10.1016/j.jpedsurg.2018.05.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29935895" target="_blank">29935895</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27544590">Inherited epidermolysis bullosa and squamous cell carcinoma: a systematic review of 117 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Montaudié H,
|
||
Chiaverini C,
|
||
Sbidian E,
|
||
Charlesworth A,
|
||
Lacour JP</span><br />
|
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<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
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2016 Aug 20;11(1):117.
|
||
doi: 10.1186/s13023-016-0489-9.
|
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<span class="bold">PMID: </span><a href="/pubmed/27544590" target="_blank">27544590</a><a href="/pmc/articles/PMC4992553" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Junctional%20epidermolysis%20bullosa%20gravis%20of%20Herlitz%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 (7)</a></div></div>
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|
||
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0079683%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (35)</a></li>
|
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<li><a href="/gtr/tests?term=C0079683%5bDISCUI%5d&filter=method%3A2%5F9" target="_blank">Sequence analysis of select exons (4)</a></li>
|
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<li><a href="/gtr/tests?term=C0079683%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (46)</a></li>
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<li><a href="/gtr/tests?term=C0079683%5bDISCUI%5d&filter=method%3A2%5F19" target="_blank">Targeted variant analysis (12)</a></li>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(junctional%20epidermolysis%20bullosa%20gravis%20of%20herlitz)%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">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Junctional%20epidermolysis%20bullosa%20gravis%20of%20Herlitz%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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<div class="portlet_content ln"><ul><li><a href="http://www.diseaseinfosearch.org/Epidermolysis+Bullosa+Letalis/2580" target="_blank">Genetic Alliance</a></li><li><a href="https://www.malacards.org/card/epidermolysis_bullosa_junctional_1b_severe" target="_blank">MalaCards</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Junctional%20epidermolysis%20bullosa%20gravis%20of%20Herlitz" target="_blank">MedlinePlus</a></li><li><a href="https://medlineplus.gov/genetics/condition/junctional-epidermolysis-bullosa" target="_blank">MedlinePlusGenetics (GHR)</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/2153/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
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