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<meta name="keywords" content="C4011556, abnormal eyebrow morphology, abnormality of the eyebrow, anatomical abnormality, eyebrow abnormalities, 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="An abnormality of the eyebrow." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=859993
|
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ConceptID=C4011556
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormal eyebrow morphology</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>859993</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:">C4011556</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Abnormality of the eyebrow</td></tr>
|
||
<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:0000534">HP:0000534</a></td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">An abnormality of the eyebrow. [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>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C4011556[DISCUI]&test_type=Clinical" ref="ncbi_uid=859993">C</a></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 Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=859993" ref="ncbi_uid=859993">V</a></span></span><span class="TLline">Abnormal eyebrow morphology</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867442" ref="tree=MeSH" title="MedGen record for Abnormality of head or neck">Abnormality of head or neck</a></span><ul><li><span class="TLline"><a href="/medgen/867438" ref="tree=MeSH" title="MedGen record for Abnormality of the head">Abnormality of the head</a></span><ul><li><span class="TLline"><a href="/medgen/871375" ref="tree=MeSH" title="MedGen record for Abnormality of the face">Abnormality of the face</a></span><ul><li><span class="TLline"><a href="/medgen/871367" ref="tree=MeSH" title="MedGen record for Abnormality of the orbital region">Abnormality of the orbital region</a></span><ul><li><span class="TLline"><a href="/medgen/1670962" ref="tree=MeSH" title="MedGen record for Abnormality of the ocular adnexa">Abnormality of the ocular adnexa</a></span><ul><li><span class="TLline"><a href="/medgen/893067" ref="tree=MeSH" title="MedGen record for Abnormal ocular adnexa morphology">Abnormal ocular adnexa morphology</a></span><ul><li><span class="matched_ds">Abnormal eyebrow morphology</span><ul><li><span class="TLline"><a href="/medgen/1372060" ref="tree=MeSH" title="MedGen record for Abnormal location of the eyebrow">Abnormal location of the eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/892938" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia of the eyebrow">Aplasia/Hypoplasia of the eyebrow</a></span><ul><li><span class="TLline"><a href="/medgen/98133" ref="tree=MeSH" title="MedGen record for Absent eyebrow">Absent eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/371332" ref="tree=MeSH" title="MedGen record for Sparse eyebrow">Sparse eyebrow</a></span><ul><li><span class="TLline"><a href="/medgen/387768" ref="tree=MeSH" title="MedGen record for Sparse lateral eyebrow">Sparse lateral eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/395444" ref="tree=MeSH" title="MedGen record for Sparse medial eyebrow">Sparse medial eyebrow</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/924116" ref="tree=MeSH" title="MedGen record for Thin eyebrow">Thin eyebrow</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/344657" ref="tree=MeSH" title="MedGen record for Broad eyebrow">Broad eyebrow</a></span><ul><li><span class="TLline"><a href="/medgen/332934" ref="tree=MeSH" title="MedGen record for Broad lateral eyebrow">Broad lateral eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/1814112" ref="tree=MeSH" title="MedGen record for Broad medial eyebrow">Broad medial eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/869291" ref="tree=MeSH" title="MedGen record for Extension of eyebrows towards upper eyelid">Extension of eyebrows towards upper eyelid</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/602077" ref="tree=MeSH" title="MedGen record for Brow ptosis">Brow ptosis</a></span></li><li><span class="TLline"><a href="/medgen/488904" ref="tree=MeSH" title="MedGen record for Double eyebrow">Double eyebrow</a></span><ul><li><span class="TLline"><a href="/medgen/868005" ref="tree=MeSH" title="MedGen record for Partial duplication of eyebrows">Partial duplication of eyebrows</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/358357" ref="tree=MeSH" title="MedGen record for Highly arched eyebrow">Highly arched eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/478649" ref="tree=MeSH" title="MedGen record for Horizontal eyebrow">Horizontal eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/375852" ref="tree=MeSH" title="MedGen record for Laterally curved eyebrow">Laterally curved eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/869034" ref="tree=MeSH" title="MedGen record for Laterally extended eyebrow">Laterally extended eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/481761" ref="tree=MeSH" title="MedGen record for Long eyebrows">Long eyebrows</a></span></li><li><span class="TLline"><a href="/medgen/336722" ref="tree=MeSH" title="MedGen record for Medial flaring of the eyebrow">Medial flaring of the eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/377914" ref="tree=MeSH" title="MedGen record for Thick eyebrow">Thick eyebrow</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<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>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_322127"><div><strong>Van den Ende-Gupta syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>322127</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.">C1833136</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Van den Ende-Gupta syndrome (VDEGS) is an autosomal recessive disorder characterized by severe contractual arachnodactyly from birth and distinctive facial dysmorphism, including triangular face, malar hypoplasia, narrow nose, everted lips, and blepharophimosis. Skeletal anomalies include slender ribs, hooked clavicles, and dislocated radial head. There is no neurologic involvement (summary by Patel et al., 2014).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/322127">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_348571"><div><strong>Autosomal dominant wooly hair</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>348571</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.">C1860238</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Woolly hair (WH) refers to a group of hair shaft disorders that are characterized by fine and tightly curled hair. Compared to normal curly hair that is observed in some populations, WH grows slowly and stops growing after a few inches. Under light microscopy, WH shows some structural anomalies, including trichorrhexis nodosa and tapered ends. WH can appear as part of several syndromes, such as Naxos disease (601214) and cardiofaciocutaneous syndrome (115150) (summary by Petukhova et al., 2009). See 278150 for a discussion of genetic heterogeneity of autosomal recessive woolly hair.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/348571">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_356704"><div><strong>Rombo syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>356704</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.">C1867147</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Rombo syndrome has characteristics of vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, and peripheral vasodilation with cyanosis and basal cell carcinomas. It has been described in four generations of one family and in two additional sporadic cases. The skin lesions become visible between 7 and 10 years of age and are most pronounced on the face. Basal cell carcinomas are frequent and develop at around 35 years of age.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/356704">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794177"><div><strong>DEGCAGS syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794177</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.">C5561967</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">DEGCAGS syndrome is an autosomal recessive syndromic neurodevelopmental disorder characterized by global developmental delay, coarse and dysmorphic facial features, and poor growth and feeding apparent from infancy. Affected individuals have variable systemic manifestations often with significant structural defects of the cardiovascular, genitourinary, gastrointestinal, and/or skeletal systems. Additional features may include sensorineural hearing loss, hypotonia, anemia or pancytopenia, and immunodeficiency with recurrent infections. Death in childhood may occur (summary by Bertoli-Avella et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794177">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_348571" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant wooly hair</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794177" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">DEGCAGS syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_356704" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Rombo syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_322127" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Van den Ende-Gupta syndrome</a></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/37166753">Keratosis pilaris: an update and approach to management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kodali N,
|
||
Patel VM,
|
||
Schwartz RA</span><br />
|
||
<span class="medgenPMjournal">Ital J Dermatol Venerol</span>
|
||
2023 Jun;158(3):217-223.
|
||
Epub 2023 May 11
|
||
doi: 10.23736/S2784-8671.23.07594-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37166753" target="_blank">37166753</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32886029">Treatment of keratosis pilaris and its variants: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Maghfour J,
|
||
Ly S,
|
||
Haidari W,
|
||
Taylor SL,
|
||
Feldman SR</span><br />
|
||
<span class="medgenPMjournal">J Dermatolog Treat</span>
|
||
2022 May;33(3):1231-1242.
|
||
Epub 2020 Sep 14
|
||
doi: 10.1080/09546634.2020.1818678.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32886029" target="_blank">32886029</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30514738">Kabuki syndrome: international consensus diagnostic criteria.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adam MP,
|
||
Banka S,
|
||
Bjornsson HT,
|
||
Bodamer O,
|
||
Chudley AE,
|
||
Harris J,
|
||
Kawame H,
|
||
Lanpher BC,
|
||
Lindsley AW,
|
||
Merla G,
|
||
Miyake N,
|
||
Okamoto N,
|
||
Stumpel CT,
|
||
Niikawa N;
|
||
Kabuki Syndrome Medical Advisory Board</span><br />
|
||
<span class="medgenPMjournal">J Med Genet</span>
|
||
2019 Feb;56(2):89-95.
|
||
Epub 2018 Dec 4
|
||
doi: 10.1136/jmedgenet-2018-105625.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30514738" target="_blank">30514738</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20eyebrow%20morphology)%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 (18)</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/31778553">Keratosis Pilaris.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Pediatr Dermatol</span>
|
||
2019 Nov;36(6):937-938.
|
||
doi: 10.1111/pde.14062.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31778553" target="_blank">31778553</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30514738">Kabuki syndrome: international consensus diagnostic criteria.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adam MP,
|
||
Banka S,
|
||
Bjornsson HT,
|
||
Bodamer O,
|
||
Chudley AE,
|
||
Harris J,
|
||
Kawame H,
|
||
Lanpher BC,
|
||
Lindsley AW,
|
||
Merla G,
|
||
Miyake N,
|
||
Okamoto N,
|
||
Stumpel CT,
|
||
Niikawa N;
|
||
Kabuki Syndrome Medical Advisory Board</span><br />
|
||
<span class="medgenPMjournal">J Med Genet</span>
|
||
2019 Feb;56(2):89-95.
|
||
Epub 2018 Dec 4
|
||
doi: 10.1136/jmedgenet-2018-105625.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30514738" target="_blank">30514738</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23850259">Poliosis circumscripta: overview and underlying causes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sleiman R,
|
||
Kurban M,
|
||
Succaria F,
|
||
Abbas O</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2013 Oct;69(4):625-33.
|
||
Epub 2013 Jul 12
|
||
doi: 10.1016/j.jaad.2013.05.022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23850259" target="_blank">23850259</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15691356">Kabuki syndrome: a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adam MP,
|
||
Hudgins L</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
2005 Mar;67(3):209-19.
|
||
doi: 10.1111/j.1399-0004.2004.00348.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15691356" target="_blank">15691356</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12925861">Ptosis: causes, presentation, and management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Finsterer J</span><br />
|
||
<span class="medgenPMjournal">Aesthetic Plast Surg</span>
|
||
2003 May-Jun;27(3):193-204.
|
||
Epub 2003 Aug 21
|
||
doi: 10.1007/s00266-003-0127-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12925861" target="_blank">12925861</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20eyebrow%20morphology%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 (107)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37166753">Keratosis pilaris: an update and approach to management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kodali N,
|
||
Patel VM,
|
||
Schwartz RA</span><br />
|
||
<span class="medgenPMjournal">Ital J Dermatol Venerol</span>
|
||
2023 Jun;158(3):217-223.
|
||
Epub 2023 May 11
|
||
doi: 10.23736/S2784-8671.23.07594-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37166753" target="_blank">37166753</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36987905">Keratosis pilaris.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Drivenes JL,
|
||
Vasilescu IC,
|
||
Bygum A</span><br />
|
||
<span class="medgenPMjournal">Tidsskr Nor Laegeforen</span>
|
||
2023 Mar 28;143(5)
|
||
Epub 2023 Mar 7
|
||
doi: 10.4045/tidsskr.22.0513.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36987905" target="_blank">36987905</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21784498">Diseases of periocular hair.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Modjtahedi BS,
|
||
Alikhan A,
|
||
Maibach HI,
|
||
Schwab IR</span><br />
|
||
<span class="medgenPMjournal">Surv Ophthalmol</span>
|
||
2011 Sep-Oct;56(5):416-32.
|
||
Epub 2011 Jul 23
|
||
doi: 10.1016/j.survophthal.2011.02.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21784498" target="_blank">21784498</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12925861">Ptosis: causes, presentation, and management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Finsterer J</span><br />
|
||
<span class="medgenPMjournal">Aesthetic Plast Surg</span>
|
||
2003 May-Jun;27(3):193-204.
|
||
Epub 2003 Aug 21
|
||
doi: 10.1007/s00266-003-0127-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12925861" target="_blank">12925861</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7996504">Fraser syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chattopadhyay A,
|
||
Kher AS,
|
||
Udwadia AD,
|
||
Sharma SV,
|
||
Bharucha BA,
|
||
Nicholson AD</span><br />
|
||
<span class="medgenPMjournal">J Postgrad Med</span>
|
||
1993 Oct-Dec;39(4):228-30.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7996504" target="_blank">7996504</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20eyebrow%20morphology%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 (221)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35976015">Keratosis Pilaris Treatment: Evidence from Intervention Studies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Suástegui-Rodríguez I,
|
||
Camacho-Rosas LH,
|
||
Peralta-Pedrero ML,
|
||
Cruz FJ,
|
||
Morales-Sánchez MA</span><br />
|
||
<span class="medgenPMjournal">Skinmed</span>
|
||
2022;20(4):258-271.
|
||
Epub 2022 Aug 31
|
||
<span class="bold">PMID: </span><a href="/pubmed/35976015" target="_blank">35976015</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31302976">Keratosis pilaris-like eruption induced by nilotinib.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jimenez-Cauhe J,
|
||
Fernandez-Gonzalez P,
|
||
Ortega-Quijano D,
|
||
Fernandez-Nieto D,
|
||
Saceda-Corralo D</span><br />
|
||
<span class="medgenPMjournal">Ital J Dermatol Venerol</span>
|
||
2021 Dec;156(Suppl. 1 to No. 6):47-48.
|
||
Epub 2019 Jul 12
|
||
doi: 10.23736/S2784-8671.19.06333-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31302976" target="_blank">31302976</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31778553">Keratosis Pilaris.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Pediatr Dermatol</span>
|
||
2019 Nov;36(6):937-938.
|
||
doi: 10.1111/pde.14062.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31778553" target="_blank">31778553</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30043128">Keratosis Pilaris and its Subtypes: Associations, New Molecular and Pharmacologic Etiologies, and Therapeutic Options.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang JF,
|
||
Orlow SJ</span><br />
|
||
<span class="medgenPMjournal">Am J Clin Dermatol</span>
|
||
2018 Oct;19(5):733-757.
|
||
doi: 10.1007/s40257-018-0368-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30043128" target="_blank">30043128</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23276366">Cutaneous toxicities of RAF inhibitors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Anforth R,
|
||
Fernandez-Peñas P,
|
||
Long GV</span><br />
|
||
<span class="medgenPMjournal">Lancet Oncol</span>
|
||
2013 Jan;14(1):e11-8.
|
||
doi: 10.1016/S1470-2045(12)70413-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23276366" target="_blank">23276366</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20eyebrow%20morphology%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 (67)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31778571">Queratosis Pilaris.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Pediatr Dermatol</span>
|
||
2019 Nov;36(6):e106-e107.
|
||
doi: 10.1111/pde.14063.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31778571" target="_blank">31778571</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31778553">Keratosis Pilaris.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Pediatr Dermatol</span>
|
||
2019 Nov;36(6):937-938.
|
||
doi: 10.1111/pde.14062.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31778553" target="_blank">31778553</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23850259">Poliosis circumscripta: overview and underlying causes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sleiman R,
|
||
Kurban M,
|
||
Succaria F,
|
||
Abbas O</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2013 Oct;69(4):625-33.
|
||
Epub 2013 Jul 12
|
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doi: 10.1016/j.jaad.2013.05.022.
|
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<span class="bold">PMID: </span><a href="/pubmed/23850259" target="_blank">23850259</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/18651971">Alpha-mannosidosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Malm D,
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||
<div class="nl"><a target="_blank" href="/pubmed/27693457">Compromized DNA repair as a basis for identification of cancer radiotherapy patients with extreme radiosensitivity.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Lobachevsky P,
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Leong T,
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Daly P,
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Smith J,
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Epub 2016 Sep 28
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<span class="bold">PMID: </span><a href="/pubmed/27693457" target="_blank">27693457</a><a href="/pmc/articles/PMC5159273" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25780981">Elejalde syndrome (ES).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mohammadzadeh Shanehsaz S,
|
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Rezazadeh A,
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Dandashli A</span><br />
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||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20eyebrow%20morphology%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 (110)</a></div></div>
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<div class="nl"><a target="_blank" href="/pubmed/32886029">Treatment of keratosis pilaris and its variants: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Maghfour J,
|
||
Ly S,
|
||
Haidari W,
|
||
Taylor SL,
|
||
Feldman SR</span><br />
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||
<span class="medgenPMjournal">J Dermatolog Treat</span>
|
||
2022 May;33(3):1231-1242.
|
||
Epub 2020 Sep 14
|
||
doi: 10.1080/09546634.2020.1818678.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32886029" target="_blank">32886029</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32804891">Light and Laser Treatments for Keratosis Pilaris: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kechichian E,
|
||
Jabbour S,
|
||
El Hachem L,
|
||
Tomb R,
|
||
Helou J</span><br />
|
||
<span class="medgenPMjournal">Dermatol Surg</span>
|
||
2020 Nov;46(11):1397-1402.
|
||
doi: 10.1097/DSS.0000000000002441.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32804891" target="_blank">32804891</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20eyebrow%20morphology%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 (2)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C4011556%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (13)</a></li>
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<li><a href="/gtr/tests?term=C4011556%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (13)</a></li>
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<p><a href="https://www.nlm.nih.gov/web_policies.html" class="text-white">Web Policies</a><br />
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<p><a class="supportLink text-white" href="https://support.nlm.nih.gov/">Help</a><br />
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