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<!--
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||
UID=598
|
||
ConceptID=C0005741
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Blepharitis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>598</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.">C0005741</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Blepharitides</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Inflammation of eyelid (1231722004); Blepharitis (41446000)</td></tr>
|
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<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0000498">HP:0000498</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0004785" target="_blank">MONDO:0004785</a></td></tr>
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</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_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">Inflammation of the eyelids. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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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">Blepharitis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/21047" ref="tree=MeSH" title="MedGen record for Pathological Conditions, Signs and Symptoms">Pathological Conditions, Signs and Symptoms</a></span><ul><li><span class="TLline"><a href="/medgen/18325" ref="tree=MeSH" title="MedGen record for Pathological process">Pathological process</a></span><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/232130" ref="tree=MeSH" title="MedGen record for Disorder by Site">Disorder by Site</a></span><ul><li><span class="TLline"><a href="/medgen/5092" ref="tree=MeSH" title="MedGen record for Disorder of eye">Disorder of eye</a></span><ul><li><span class="TLline"><a href="/medgen/41938" ref="tree=MeSH" title="MedGen record for Eyelid disorder">Eyelid disorder</a></span><ul><li><span class="matched_ds">Blepharitis</span><ul><li><span class="TLline"><a href="/medgen/1632973" ref="tree=MeSH" title="MedGen record for Anterior blepharitis">Anterior blepharitis</a></span></li><li><span class="TLline"><a href="/medgen/698924" ref="tree=MeSH" title="MedGen record for Posterior blepharitis">Posterior blepharitis</a></span><ul><li><span class="TLline"><a href="/medgen/508440" ref="tree=MeSH" title="MedGen record for Seborrhoeic blepharitis">Seborrhoeic blepharitis</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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<div class="portlet mgSection" id="ID_112">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln clinfeat">
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||
<div class="divPopper rprt" id="rdis_56416"><div><strong>Hidrotic ectodermal dysplasia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>56416</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."><span class="highlight" style="background-color:">C0162361</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hidrotic ectodermal dysplasia 2, or Clouston syndrome (referred to as HED2 throughout this GeneReview) is characterized by a triad of major clinical features including partial-to-complete alopecia, nail dystrophy, and palmoplantar hyperkeratosis. Sweating is preserved and there are usually no dental anomalies. Sparse scalp hair and dysplastic nails are seen early in life. In infancy, scalp hair is fine, sparse, and brittle. Progressive hair loss may lead to total alopecia by puberty. The nails may be milky white in early childhood; they gradually become dystrophic, thick, and distally separated from the nail bed. Palmoplantar keratoderma may develop during childhood and increases in severity with age. Associated features may include cutaneous hyperpigmentation (particularly over the joints) and finger clubbing. The clinical manifestations are highly variable even within the same family.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/56416">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_98032"><div><strong>Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>98032</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.">C0406709</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The TP63-related disorders comprise six overlapping phenotypes: Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome (which includes Rapp-Hodgkin syndrome). Acro-dermo-ungual-lacrimal-tooth (ADULT) syndrome. Ectrodactyly, ectodermal dysplasia, cleft lip/palate syndrome 3 (EEC3). Limb-mammary syndrome. Split-hand/foot malformation type 4 (SHFM4). Isolated cleft lip/cleft palate (orofacial cleft 8). Individuals typically have varying combinations of ectodermal dysplasia (hypohidrosis, nail dysplasia, sparse hair, tooth abnormalities), cleft lip/palate, split-hand/foot malformation/syndactyly, lacrimal duct obstruction, hypopigmentation, hypoplastic breasts and/or nipples, and hypospadias. Findings associated with a single phenotype include ankyloblepharon filiforme adnatum (tissue strands that completely or partially fuse the upper and lower eyelids), skin erosions especially on the scalp associated with areas of scarring, and alopecia, trismus, and excessive freckling.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/98032">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_216941"><div><strong>Dyskeratosis congenita, X-linked</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>216941</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.">C1148551</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Dyskeratosis congenita and related telomere biology disorders (DC/TBD) are caused by impaired telomere maintenance resulting in short or very short telomeres. The phenotypic spectrum of telomere biology disorders is broad and includes individuals with classic dyskeratosis congenita (DC) as well as those with very short telomeres and an isolated physical finding. Classic DC is characterized by a triad of dysplastic nails, lacy reticular pigmentation of the upper chest and/or neck, and oral leukoplakia, although this may not be present in all individuals. People with DC/TBD are at increased risk for progressive bone marrow failure (BMF), myelodysplastic syndrome or acute myelogenous leukemia, solid tumors (usually squamous cell carcinoma of the head/neck or anogenital cancer), and pulmonary fibrosis. Other findings can include eye abnormalities (epiphora, blepharitis, sparse eyelashes, ectropion, entropion, trichiasis), taurodontism, liver disease, gastrointestinal telangiectasias, and avascular necrosis of the hips or shoulders. Although most persons with DC/TBD have normal psychomotor development and normal neurologic function, significant developmental delay is present in both forms; additional findings include cerebellar hypoplasia (Hoyeraal Hreidarsson syndrome) and bilateral exudative retinopathy and intracranial calcifications (Revesz syndrome and Coats plus syndrome). Onset and progression of manifestations of DC/TBD vary: at the mild end of the spectrum are those who have only minimal physical findings with normal bone marrow function, and at the severe end are those who have the diagnostic triad and early-onset BMF.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/216941">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_332073"><div><strong>Autosomal recessive congenital ichthyosis 11</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>332073</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.">C1835851</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of disorders of keratinization characterized primarily by abnormal skin scaling over the whole body. These disorders are limited to skin, with approximately two-thirds of patients presenting severe symptoms. The main skin phenotypes are lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE), although phenotypic overlap within the same patient or among patients from the same family can occur (summary by Fischer, 2009). Neither histopathologic findings nor ultrastructural features clearly distinguish between NCIE and LI. In addition, mutations in several genes have been shown to cause both lamellar and nonbullous ichthyosiform erythrodermal phenotypes (Akiyama et al., 2003). At the First Ichthyosis Consensus Conference in Soreze in 2009, the term 'autosomal recessive congenital ichthyosis' (ARCI) was designated to encompass LI, NCIE, and harlequin ichthyosis (ARCI4B; 242500) (Oji et al., 2010). NCIE is characterized by prominent erythroderma and fine white, superficial, semiadherent scales. Most patients present with collodion membrane at birth and have palmoplantar keratoderma, often with painful fissures, digital contractures, and loss of pulp volume. In half of the cases, a nail dystrophy including ridging, subungual hyperkeratosis, or hypoplasia has been described. Ectropion, eclabium, scalp involvement, and loss of eyebrows and lashes seem to be more frequent in NCIE than in lamellar ichthyosis (summary by Fischer et al., 2000). In LI, the scales are large, adherent, dark, and pigmented with no skin erythema. Overlapping phenotypes may depend on the age of the patient and the region of the body. The terminal differentiation of the epidermis is perturbed in both forms, leading to reduced barrier function and defects of lipid composition in the stratum corneum (summary by Lefevre et al., 2006). In later life, the skin in ARCI may have scales that cover the entire body surface, including the flexural folds, and the scales are highly variable in size and color. Erythema may be very mild and almost invisible. Some affected persons exhibit scarring alopecia, and many have secondary anhidrosis (summary by Eckl et al., 2005). For a general phenotypic description and discussion of genetic heterogeneity of autosomal recessive congenital ichthyosis, see ARCI1 (242300).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/332073">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_343663"><div><strong>Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>343663</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.">C1851841</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An EEC syndrome characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 7q11.2-q21.3.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/343663">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_347666"><div><strong>Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347666</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.">C1858562</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The TP63-related disorders comprise six overlapping phenotypes: Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome (which includes Rapp-Hodgkin syndrome). Acro-dermo-ungual-lacrimal-tooth (ADULT) syndrome. Ectrodactyly, ectodermal dysplasia, cleft lip/palate syndrome 3 (EEC3). Limb-mammary syndrome. Split-hand/foot malformation type 4 (SHFM4). Isolated cleft lip/cleft palate (orofacial cleft 8). Individuals typically have varying combinations of ectodermal dysplasia (hypohidrosis, nail dysplasia, sparse hair, tooth abnormalities), cleft lip/palate, split-hand/foot malformation/syndactyly, lacrimal duct obstruction, hypopigmentation, hypoplastic breasts and/or nipples, and hypospadias. Findings associated with a single phenotype include ankyloblepharon filiforme adnatum (tissue strands that completely or partially fuse the upper and lower eyelids), skin erosions especially on the scalp associated with areas of scarring, and alopecia, trismus, and excessive freckling.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/347666">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_388129"><div><strong>Poikiloderma with neutropenia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>388129</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.">C1858723</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Poikiloderma with neutropenia (PN) is characterized by an inflammatory eczematous rash (appears at ages 6-12 months) followed by post-inflammatory poikiloderma (at age >2 years) and chronic noncyclic neutropenia typically associated with recurrent sinopulmonary infections in the first two years of life and (often) bronchiectasis. There is increased risk for myelodysplastic syndrome, acute myelogenous leukemia, and skin cancer. Other ectodermal findings include thickened nails, nail dystrophy, and palmar/plantar hyperkeratosis. Most affected individuals also have reactive airway disease, and some have short stature, hypogonadotropic hypogonadism, midfacial retrusion, calcinosis cutis, and non-healing skin ulcers.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/388129">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_412573"><div><strong>Keratosis follicularis spinulosa decalvans, autosomal dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>412573</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.">C2748527</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Keratosis follicularis spinulosa decalvans (KFSD) is an uncommon genodermatosis characterized by follicular hyperkeratosis, progressive cicatricial alopecia, and photophobia. Most reported cases show X-linked inheritance (KFSDX; 308800) (Castori et al., 2009).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/412573">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_482131"><div><strong>Inflammatory skin and bowel disease, neonatal, 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>482131</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.">C3280501</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any neonatal inflammatory skin and bowel disease in which the cause of the disease is a mutation in the ADAM17 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/482131">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_811541"><div><strong>Candidiasis, familial, 8</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>811541</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.">C3714992</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Chronic mucocutaneous candidiasis is characterized by recurrent or persistent infections of the skin, nails, and oral and genital mucosae with Candida albicans, and sometimes by staphylococcal skin infections (summary by Boisson et al., 2013). For a discussion of genetic heterogeneity of familial candidiasis, see CANDF1 (114580).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/811541">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_813075"><div><strong>Olmsted syndrome, X-linked</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>813075</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.">C3806745</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">X-linked Olmsted syndrome (OLMSX) is a rare keratinization disorder characterized by the combination of periorificial keratotic plaques and bilateral palmoplantar transgredient keratoderma. Other clinical manifestations include diffuse alopecia, leukokeratosis of the oral mucosa, onychodystrophy, hyperkeratotic linear streaks, follicular keratosis, and constriction of the digits (summary by Yaghoobi et al., 2007). For a general phenotypic description and a discussion of genetic heterogeneity of Olmsted disease, see OLMS1 (614594).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/813075">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_854384"><div><strong>Keratosis follicularis spinulosa decalvans, X-linked</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>854384</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.">C3887525</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Keratosis follicularis spinulosa decalvans is an uncommon genodermatosis chiefly characterized by widespread keratosis pilaris, progressive cicatricial alopecia of the scalp, eyebrows, and eyelashes, and an excess of affected males. Photophobia, blepharitis/conjunctivitis, and corneal dystrophy are characteristic ancillary findings. It is most often inherited as an X-linked trait (summary by Castori et al., 2009). Autosomal dominant inheritance has also been reported (KFSD; 612843). The term 'cum ophiasi' means 'with ophiasis,' i.e., baldness in 1 or more winding streaks about the head, which comes from the Greek for snake. Decalvans refers to the loss of hair.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/854384">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1381460"><div><strong>Immunoskeletal dysplasia with neurodevelopmental abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1381460</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.">C4479452</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1381460">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1618052"><div><strong>Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1618052</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.">C4540232</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Immunodeficiency-71 with inflammatory disease and congenital thrombocytopenia (IMD71) is an autosomal recessive immunologic disorder characterized by the onset of recurrent infections and inflammatory features such as vasculitis and eczema in infancy or early childhood. Infectious agents include bacteria and viruses. Laboratory findings are variable, but usually show thrombocytopenia, sometimes with abnormal platelet morphology, increased serum IgE, IgA, or IgM, leukocytosis, decreased or increased T lymphocytes, and increased eosinophils. Detailed studies show impaired neutrophil and T-cell chemotaxis, as well as impaired T-cell activation due to defects in F-actin (see 102610) polymerization (summary by Brigida et al., 2018).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1618052">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1680605"><div><strong>Ectodermal dysplasia 15, hypohidrotic/hair type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1680605</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.">C5193145</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Some ectodermal dysplasias are here classified as congenital disorders characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings. Ectodermal dysplasia-15 (ECTD15) is characterized by hypotrichosis that develops in early childhood and absence of sweating except with extreme exercise. Skin is dry from birth and eczematous lesions may develop in adulthood. Other features include blepharitis and photophobia (van den Bogaard et al., 2019).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1680605">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1798933"><div><strong>Microcephaly-congenital cataract-psoriasiform dermatitis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1798933</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.">C5567510</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Microcephaly, congenital cataract, and psoriasiform dermatitis (MCCPD) represents an inborn error of cholesterol metabolism that is characterized by accumulation of a large amount of methylsterols, particularly dimethylsterols, in affected patients. The associated features of immune dysregulation, skin disease, and growth delay can be at least partially corrected with cholesterol and statin supplements (He et al., 2014).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1798933">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_98032" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_332073" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive congenital ichthyosis 11</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_811541" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Candidiasis, familial, 8</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_216941" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Dyskeratosis congenita, X-linked</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1680605" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ectodermal dysplasia 15, hypohidrotic/hair type</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (16)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_343663" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_347666" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_56416" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hidrotic ectodermal dysplasia syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1381460" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunoskeletal dysplasia with neurodevelopmental abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_482131" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Inflammatory skin and bowel disease, neonatal, 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_412573" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Keratosis follicularis spinulosa decalvans, autosomal dominant</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_854384" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Keratosis follicularis spinulosa decalvans, X-linked</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1798933" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Microcephaly-congenital cataract-psoriasiform dermatitis syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_813075" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Olmsted syndrome, X-linked</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1618052" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_388129" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Poikiloderma with neutropenia</a></div></span></div></div>
|
||
</div>
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|
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<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/38349296">Blepharitis Preferred Practice Pattern®.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lin A,
|
||
Ahmad S,
|
||
Amescua G,
|
||
Cheung AY,
|
||
Choi DS,
|
||
Jhanji V,
|
||
Mian SI,
|
||
Rhee MK,
|
||
Viriya ET,
|
||
Mah FS,
|
||
Varu DM;
|
||
American Academy of Ophthalmology Preferred Practice Pattern Cornea/External Disease Panel</span><br />
|
||
<span class="medgenPMjournal">Ophthalmology</span>
|
||
2024 Apr;131(4):P50-P86.
|
||
Epub 2024 Feb 13
|
||
doi: 10.1016/j.ophtha.2023.12.036.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38349296" target="_blank">38349296</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31494111">Management of meibomian gland dysfunction: a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sabeti S,
|
||
Kheirkhah A,
|
||
Yin J,
|
||
Dana R</span><br />
|
||
<span class="medgenPMjournal">Surv Ophthalmol</span>
|
||
2020 Mar-Apr;65(2):205-217.
|
||
Epub 2019 Sep 5
|
||
doi: 10.1016/j.survophthal.2019.08.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31494111" target="_blank">31494111</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30366800">Blepharitis Preferred Practice Pattern®.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Amescua G,
|
||
Akpek EK,
|
||
Farid M,
|
||
Garcia-Ferrer FJ,
|
||
Lin A,
|
||
Rhee MK,
|
||
Varu DM,
|
||
Musch DC,
|
||
Dunn SP,
|
||
Mah FS;
|
||
American Academy of Ophthalmology Preferred Practice Pattern Cornea and External Disease Panel</span><br />
|
||
<span class="medgenPMjournal">Ophthalmology</span>
|
||
2019 Jan;126(1):P56-P93.
|
||
Epub 2018 Oct 23
|
||
doi: 10.1016/j.ophtha.2018.10.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30366800" target="_blank">30366800</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22blepharitis%22%5Btiab%3A~0%5D)%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 (107)</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/38814581">Ocular toxicities associated with antibody drug conjugates.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marshall RF,
|
||
Xu H,
|
||
Berkenstock M</span><br />
|
||
<span class="medgenPMjournal">Curr Opin Ophthalmol</span>
|
||
2024 Nov 1;35(6):494-498.
|
||
Epub 2024 May 30
|
||
doi: 10.1097/ICU.0000000000001063.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38814581" target="_blank">38814581</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37937798">Chalazion Treatment: A Concise Review of Clinical Trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tashbayev B,
|
||
Chen X,
|
||
Utheim TP</span><br />
|
||
<span class="medgenPMjournal">Curr Eye Res</span>
|
||
2024 Feb;49(2):109-118.
|
||
Epub 2024 Jan 18
|
||
doi: 10.1080/02713683.2023.2279014.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37937798" target="_blank">37937798</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37272680">Demodex Blepharitis: A Comprehensive Review of the Disease, Current Management, and Emerging Therapies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rhee MK,
|
||
Yeu E,
|
||
Barnett M,
|
||
Rapuano CJ,
|
||
Dhaliwal DK,
|
||
Nichols KK,
|
||
Karpecki P,
|
||
Mah FS,
|
||
Chan A,
|
||
Mun J,
|
||
Gaddie IB</span><br />
|
||
<span class="medgenPMjournal">Eye Contact Lens</span>
|
||
2023 Aug 1;49(8):311-318.
|
||
Epub 2023 Jun 2
|
||
doi: 10.1097/ICL.0000000000001003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37272680" target="_blank">37272680</a><a href="/pmc/articles/PMC10351901" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34743107">Update on the Management of Demodex Blepharitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shah PP,
|
||
Stein RL,
|
||
Perry HD</span><br />
|
||
<span class="medgenPMjournal">Cornea</span>
|
||
2022 Aug 1;41(8):934-939.
|
||
Epub 2021 Nov 3
|
||
doi: 10.1097/ICO.0000000000002911.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34743107" target="_blank">34743107</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8500319">Keratoglobus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cameron JA</span><br />
|
||
<span class="medgenPMjournal">Cornea</span>
|
||
1993 Mar;12(2):124-30.
|
||
doi: 10.1097/00003226-199303000-00006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8500319" target="_blank">8500319</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Blepharitis%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 (667)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33403718">Ocular manifestations of rosacea: A clinical review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tavassoli S,
|
||
Wong N,
|
||
Chan E</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Ophthalmol</span>
|
||
2021 Mar;49(2):104-117.
|
||
Epub 2021 Feb 3
|
||
doi: 10.1111/ceo.13900.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33403718" target="_blank">33403718</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30366800">Blepharitis Preferred Practice Pattern®.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Amescua G,
|
||
Akpek EK,
|
||
Farid M,
|
||
Garcia-Ferrer FJ,
|
||
Lin A,
|
||
Rhee MK,
|
||
Varu DM,
|
||
Musch DC,
|
||
Dunn SP,
|
||
Mah FS;
|
||
American Academy of Ophthalmology Preferred Practice Pattern Cornea and External Disease Panel</span><br />
|
||
<span class="medgenPMjournal">Ophthalmology</span>
|
||
2019 Jan;126(1):P56-P93.
|
||
Epub 2018 Oct 23
|
||
doi: 10.1016/j.ophtha.2018.10.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30366800" target="_blank">30366800</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26058029">Blepharokeratoconjunctivitis in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hammersmith KM</span><br />
|
||
<span class="medgenPMjournal">Curr Opin Ophthalmol</span>
|
||
2015 Jul;26(4):301-5.
|
||
doi: 10.1097/ICU.0000000000000167.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26058029" target="_blank">26058029</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1460263">Infectious conjunctivitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Syed NA,
|
||
Hyndiuk RA</span><br />
|
||
<span class="medgenPMjournal">Infect Dis Clin North Am</span>
|
||
1992 Dec;6(4):789-805.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1460263" target="_blank">1460263</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/324453">Staphylococcal blepharitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Smolin G,
|
||
Okumoto M</span><br />
|
||
<span class="medgenPMjournal">Arch Ophthalmol</span>
|
||
1977 May;95(5):812-6.
|
||
doi: 10.1001/archopht.1977.04450050090009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/324453" target="_blank">324453</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Blepharitis%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 (780)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37272680">Demodex Blepharitis: A Comprehensive Review of the Disease, Current Management, and Emerging Therapies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rhee MK,
|
||
Yeu E,
|
||
Barnett M,
|
||
Rapuano CJ,
|
||
Dhaliwal DK,
|
||
Nichols KK,
|
||
Karpecki P,
|
||
Mah FS,
|
||
Chan A,
|
||
Mun J,
|
||
Gaddie IB</span><br />
|
||
<span class="medgenPMjournal">Eye Contact Lens</span>
|
||
2023 Aug 1;49(8):311-318.
|
||
Epub 2023 Jun 2
|
||
doi: 10.1097/ICL.0000000000001003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37272680" target="_blank">37272680</a><a href="/pmc/articles/PMC10351901" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34743107">Update on the Management of Demodex Blepharitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shah PP,
|
||
Stein RL,
|
||
Perry HD</span><br />
|
||
<span class="medgenPMjournal">Cornea</span>
|
||
2022 Aug 1;41(8):934-939.
|
||
Epub 2021 Nov 3
|
||
doi: 10.1097/ICO.0000000000002911.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34743107" target="_blank">34743107</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30366800">Blepharitis Preferred Practice Pattern®.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Amescua G,
|
||
Akpek EK,
|
||
Farid M,
|
||
Garcia-Ferrer FJ,
|
||
Lin A,
|
||
Rhee MK,
|
||
Varu DM,
|
||
Musch DC,
|
||
Dunn SP,
|
||
Mah FS;
|
||
American Academy of Ophthalmology Preferred Practice Pattern Cornea and External Disease Panel</span><br />
|
||
<span class="medgenPMjournal">Ophthalmology</span>
|
||
2019 Jan;126(1):P56-P93.
|
||
Epub 2018 Oct 23
|
||
doi: 10.1016/j.ophtha.2018.10.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30366800" target="_blank">30366800</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1460263">Infectious conjunctivitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Syed NA,
|
||
Hyndiuk RA</span><br />
|
||
<span class="medgenPMjournal">Infect Dis Clin North Am</span>
|
||
1992 Dec;6(4):789-805.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1460263" target="_blank">1460263</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/324453">Staphylococcal blepharitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Smolin G,
|
||
Okumoto M</span><br />
|
||
<span class="medgenPMjournal">Arch Ophthalmol</span>
|
||
1977 May;95(5):812-6.
|
||
doi: 10.1001/archopht.1977.04450050090009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/324453" target="_blank">324453</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Blepharitis%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 (707)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35275334">Dupilumab-Associated Adverse Events During Treatment of Allergic Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kychygina A,
|
||
Cassagne M,
|
||
Tauber M,
|
||
Galiacy S,
|
||
Paul C,
|
||
Fournié P,
|
||
Simon M</span><br />
|
||
<span class="medgenPMjournal">Clin Rev Allergy Immunol</span>
|
||
2022 Jun;62(3):519-533.
|
||
Epub 2022 Mar 11
|
||
doi: 10.1007/s12016-022-08934-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35275334" target="_blank">35275334</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26058029">Blepharokeratoconjunctivitis in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hammersmith KM</span><br />
|
||
<span class="medgenPMjournal">Curr Opin Ophthalmol</span>
|
||
2015 Jul;26(4):301-5.
|
||
doi: 10.1097/ICU.0000000000000167.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26058029" target="_blank">26058029</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24342754">Atopic keratoconjunctivitis: A review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen JJ,
|
||
Applebaum DS,
|
||
Sun GS,
|
||
Pflugfelder SC</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2014 Mar;70(3):569-75.
|
||
Epub 2013 Dec 15
|
||
doi: 10.1016/j.jaad.2013.10.036.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24342754" target="_blank">24342754</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15807644">Is it blepharitis?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Swann PG,
|
||
Weir J</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Optom</span>
|
||
2005 Mar;88(2):113-4.
|
||
doi: 10.1111/j.1444-0938.2005.tb06677.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15807644" target="_blank">15807644</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3116121">Noma neonatorum.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Borle RM,
|
||
Agrawal M</span><br />
|
||
<span class="medgenPMjournal">Int J Oral Maxillofac Surg</span>
|
||
1987 Oct;16(5):626-9.
|
||
doi: 10.1016/s0901-5027(87)80118-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3116121" target="_blank">3116121</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Blepharitis%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 (257)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38554594">Orbital/ocular inflammatory involvement in VEXAS syndrome: Data from the international AIDA network VEXAS registry.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vitale A,
|
||
Caggiano V,
|
||
Martin-Nares E,
|
||
Frassi M,
|
||
Dagna L,
|
||
Hissaria P,
|
||
Sfriso P,
|
||
Hernández-Rodríguez J,
|
||
Ruiz-Irastorza G,
|
||
Monti S,
|
||
Tufan A,
|
||
Piga M,
|
||
Giardini HAM,
|
||
Lopalco G,
|
||
Viapiana O,
|
||
De Paulis A,
|
||
Triggianese P,
|
||
Vitetta R,
|
||
de-la-Torre A,
|
||
Fonollosa A,
|
||
Caroni F,
|
||
Sota J,
|
||
Conticini E,
|
||
Sbalchiero J,
|
||
Renieri A,
|
||
Casamassima G,
|
||
Wiesik-Szewczyk E,
|
||
Yildirim D,
|
||
Hinojosa-Azaola A,
|
||
Crisafulli F,
|
||
Franceschini F,
|
||
Campochiaro C,
|
||
Tomelleri A,
|
||
Callisto A,
|
||
Beecher M,
|
||
Bindoli S,
|
||
Baggio C,
|
||
Gómez-Caverzaschi V,
|
||
Pelegrín L,
|
||
Soto-Peleteiro A,
|
||
Milanesi A,
|
||
Vasi I,
|
||
Cauli A,
|
||
Antonelli IPB,
|
||
Iannone F,
|
||
Bixio R,
|
||
Casa FD,
|
||
Mormile I,
|
||
Gurnari C,
|
||
Fiorenza A,
|
||
Mejia-Salgado G,
|
||
Kawakami-Campos PA,
|
||
Ragab G,
|
||
Ciccia F,
|
||
Ruscitti P,
|
||
Bocchia M,
|
||
Balistreri A,
|
||
Tosi GM,
|
||
Frediani B,
|
||
Cantarini L,
|
||
Fabiani C</span><br />
|
||
<span class="medgenPMjournal">Semin Arthritis Rheum</span>
|
||
2024 Jun;66:152430.
|
||
Epub 2024 Mar 18
|
||
doi: 10.1016/j.semarthrit.2024.152430.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38554594" target="_blank">38554594</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36310014">Comparison of Different Anti-Demodex Strategies: A Systematic Review and Meta-Analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Li J,
|
||
Wei E,
|
||
Reisinger A,
|
||
French LE,
|
||
Clanner-Engelshofen BM,
|
||
Reinholz M</span><br />
|
||
<span class="medgenPMjournal">Dermatology</span>
|
||
2023;239(1):12-31.
|
||
Epub 2022 Oct 28
|
||
doi: 10.1159/000526296.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36310014" target="_blank">36310014</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35275334">Dupilumab-Associated Adverse Events During Treatment of Allergic Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kychygina A,
|
||
Cassagne M,
|
||
Tauber M,
|
||
Galiacy S,
|
||
Paul C,
|
||
Fournié P,
|
||
Simon M</span><br />
|
||
<span class="medgenPMjournal">Clin Rev Allergy Immunol</span>
|
||
2022 Jun;62(3):519-533.
|
||
Epub 2022 Mar 11
|
||
doi: 10.1007/s12016-022-08934-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35275334" target="_blank">35275334</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32822798">Real-world evidence of dupilumab efficacy and risk of adverse events: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Halling AS,
|
||
Loft N,
|
||
Silverberg JI,
|
||
Guttman-Yassky E,
|
||
Thyssen JP</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2021 Jan;84(1):139-147.
|
||
Epub 2020 Aug 18
|
||
doi: 10.1016/j.jaad.2020.08.051.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32822798" target="_blank">32822798</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15807644">Is it blepharitis?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Swann PG,
|
||
Weir J</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Optom</span>
|
||
2005 Mar;88(2):113-4.
|
||
doi: 10.1111/j.1444-0938.2005.tb06677.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15807644" target="_blank">15807644</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Blepharitis%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 (374)</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/37596128">Treatment of pediatric ocular rosacea: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Khaslavsky S,
|
||
Starkey SY,
|
||
Avraham S,
|
||
Kashetsky N,
|
||
Mukovozov I</span><br />
|
||
<span class="medgenPMjournal">Ann Dermatol Venereol</span>
|
||
2023 Sep;150(3):199-201.
|
||
Epub 2023 Aug 16
|
||
doi: 10.1016/j.annder.2023.05.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37596128" target="_blank">37596128</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36310014">Comparison of Different Anti-Demodex Strategies: A Systematic Review and Meta-Analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Li J,
|
||
Wei E,
|
||
Reisinger A,
|
||
French LE,
|
||
Clanner-Engelshofen BM,
|
||
Reinholz M</span><br />
|
||
<span class="medgenPMjournal">Dermatology</span>
|
||
2023;239(1):12-31.
|
||
Epub 2022 Oct 28
|
||
doi: 10.1159/000526296.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36310014" target="_blank">36310014</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32822798">Real-world evidence of dupilumab efficacy and risk of adverse events: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Halling AS,
|
||
Loft N,
|
||
Silverberg JI,
|
||
Guttman-Yassky E,
|
||
Thyssen JP</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2021 Jan;84(1):139-147.
|
||
Epub 2020 Aug 18
|
||
doi: 10.1016/j.jaad.2020.08.051.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32822798" target="_blank">32822798</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30668185">Topical ketoconazole: a systematic review of current dermatological applications and future developments.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Choi FD,
|
||
Juhasz MLW,
|
||
Atanaskova Mesinkovska N</span><br />
|
||
<span class="medgenPMjournal">J Dermatolog Treat</span>
|
||
2019 Dec;30(8):760-771.
|
||
Epub 2019 Feb 14
|
||
doi: 10.1080/09546634.2019.1573309.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30668185" target="_blank">30668185</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30561146">Effectiveness of pharmaceutical interventions for meibomian gland dysfunction: An evidence-based review of clinical trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Khoo P,
|
||
Ooi KG,
|
||
Watson S</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Ophthalmol</span>
|
||
2019 Jul;47(5):658-668.
|
||
Epub 2019 Feb 18
|
||
doi: 10.1111/ceo.13460.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30561146" target="_blank">30561146</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Blepharitis%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 (24)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
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<div class="portlet mgSection" id="ID_113">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul id="my-toc"></ul></div>
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||
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Blepharitis" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_121">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22blepharitis%22%5Btiab%3A~0%5D)%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(%22Blepharitis%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 mgSection" id="ID_116">
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||
<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Blepharitis" target="_blank">MedlinePlus</a></li></ul></div>
|
||
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|
||
</div>
|
||
<div class="portlet brieflink">
|
||
<div class="portlet_head">
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<div class="portlet_title">
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<h3>Reviews</h3>
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenReviews.Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="Reviews" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenReviews.Shutter"></a>
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<div class="portlet_content">
|
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<ul>
|
||
<li>
|
||
<a href="/pubmed/clinical?term=Blepharitis" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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</li>
|
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<li>
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||
<a href="/pubmed?term=Blepharitis%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
|
||
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|
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|
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|
||
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<!-- MedGen supplemental column ends here -->
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<h3>Related information</h3>
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<div class="portlet_content DiscoveryDbLinks">
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<ul>
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<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/mesh?LinkName=medgen_mesh&from_uid=598" ref="log$=recordlinks">MeSH</a>
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<div class="brieflinkpop offscreen_noflow">Related Medical Subject Headings</div>
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</li>
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<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=598" ref="log$=recordlinks">PMC Articles</a>
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<div class="brieflinkpop offscreen_noflow">Related information in PubMed Central Links</div>
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<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=598" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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||
</ul>
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||
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||
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||
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||
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<h3>Recent activity</h3>
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" cmd="ClearHT" href="?cmd=ClearHT&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory">
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Clear
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" class="HTOn" cmd="HTOff" href="?cmd=HTOff&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle">
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Turn Off
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Turn On
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<ul id="activity">
|
||
<li class="ra_rcd ralinkpopper two_line">
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d44dae84f3725e59cf4b90">Blepharitis</a>
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||
<div class="ralinkpop offscreen_noflow">Blepharitis<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
|
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</li>
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<li class="ra_rcd ralinkpopper two_line">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d44dac84f3725e59cf4552">Abnormal foot morphology</a>
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<div class="ralinkpop offscreen_noflow">Abnormal foot morphology<div class="brieflinkpopdesc"></div></div>
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||
<div class="tertiary">MedGen</div>
|
||
</li>
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||
<li class="ra_rcd ralinkpopper two_line">
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d44daa2f30673f7b8b8804">Palmoplantar keratosis</a>
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<div class="ralinkpop offscreen_noflow">Palmoplantar keratosis<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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</li>
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<li class="ra_rcd ralinkpopper two_line">
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=4" href="/portal/utils/pageresolver.fcgi?recordid=67d44da684f3725e59cf260f">Hidrotic Ectodermal Dysplasia 2 - GeneReviews®</a>
|
||
<div class="ralinkpop offscreen_noflow">Hidrotic Ectodermal Dysplasia 2 - GeneReviews®<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary"></div>
|
||
</li>
|
||
<li class="ra_rcd ralinkpopper two_line">
|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=5" href="/portal/utils/pageresolver.fcgi?recordid=67d44da567c23b31e046439d">Table B. [OMIM Entries for Hidrotic Ectodermal Dysplasia 2 (View All in OMIM)]. ...</a>
|
||
<div class="ralinkpop offscreen_noflow">Table B. [OMIM Entries for Hidrotic Ectodermal Dysplasia 2 (View All in OMIM)]. - GeneReviews®<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary"></div>
|
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