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<!--
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UID=869296
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ConceptID=C4023722
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormality of hair texture</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>869296</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.">C4023722</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Abnormality of hair consistency; Abnormality of hair curl pattern; Abnormality of hair volume</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0010719">HP:0010719</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>
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||
<div class="portlet_content ln">An abnormality of the texture of the hair. [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 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">Abnormality of hair texture</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/871273" ref="tree=MeSH" title="MedGen record for Abnormality of the integument">Abnormality of the integument</a></span><ul><li><span class="TLline"><a href="/medgen/869100" ref="tree=MeSH" title="MedGen record for Abnormal skin adnexa morphology">Abnormal skin adnexa morphology</a></span><ul><li><span class="TLline"><a href="/medgen/56381" ref="tree=MeSH" title="MedGen record for Abnormal hair morphology">Abnormal hair morphology</a></span><ul><li><span class="matched_ds">Abnormality of hair texture</span><ul><li><span class="TLline"><a href="/medgen/120480" ref="tree=MeSH" title="MedGen record for Brittle hair">Brittle hair</a></span><ul><li><span class="TLline"><a href="/medgen/870836" ref="tree=MeSH" title="MedGen record for Brittle scalp hair">Brittle scalp hair</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/124454" ref="tree=MeSH" title="MedGen record for Coarse hair">Coarse hair</a></span></li><li><span class="TLline"><a href="/medgen/488919" ref="tree=MeSH" title="MedGen record for Curly hair">Curly hair</a></span></li><li><span class="TLline"><a href="/medgen/75809" ref="tree=MeSH" title="MedGen record for Dry hair">Dry hair</a></span></li><li><span class="TLline"><a href="/medgen/98401" ref="tree=MeSH" title="MedGen record for Fine hair">Fine hair</a></span></li><li><span class="TLline"><a href="/medgen/348660" ref="tree=MeSH" title="MedGen record for Uncombable hair">Uncombable hair</a></span></li><li><span class="TLline"><a href="/medgen/87469" ref="tree=MeSH" title="MedGen record for Wooly hair">Wooly hair</a></span><ul><li><span class="TLline"><a href="/medgen/348571" ref="tree=MeSH" title="MedGen record for Autosomal dominant wooly hair">Autosomal dominant wooly hair</a></span></li><li><span class="TLline"><a href="/medgen/481100" ref="tree=MeSH" title="MedGen record for Hypotrichosis 8">Hypotrichosis 8</a></span></li><li><span class="TLline"><a href="/medgen/863640" ref="tree=MeSH" title="MedGen record for Woolly scalp hair">Woolly scalp hair</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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||
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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>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_82795"><div><strong>Cutis laxa with osteodystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>82795</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.">C0268355</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">ATP6V0A2-related cutis laxa is characterized by generalized cutis laxa, findings associated with generalized connective tissue disorder, developmental delays, and a variety of neurologic findings including abnormality on brain MRI. At birth, hypotonia, overfolded skin, and distinctive facial features are present and enlarged fontanelles are often observed. During childhood, the characteristic facial features and thick or coarse hair may become quite pronounced. The skin findings decrease with age, although easy bruising and Ehlers-Danlos-like scars have been described in some. In most (not all) affected individuals, cortical and cerebellar malformations are observed on brain MRI. Nearly all affected individuals have developmental delays, seizures, and neurologic regression.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/82795">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_108185"><div><strong>Beaded hair</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>108185</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.">C0546966</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Individuals with monilethrix have normal hair at birth, but within the first few months of life develop fragile, brittle hair that tends to fracture and produce varying degrees of dystrophic alopecia. In the mildest forms, only the occipital regions of the scalp are involved; however, in severe forms the eyebrows, eyelashes, and secondary sexual hair may also be involved. Follicular hyperkeratosis with predilection for the scalp, nape of neck, and extensor surfaces of the upper arm and thighs is also a characteristic finding in these patients. Light microscopic examination is diagnostic and reveals elliptical nodes of normal thickness and intermittent constrictions (internodes) at which the hair easily breaks. There may be spontaneous improvement with time, especially during puberty and pregnancy, but the condition never resolves completely (summary by Zlotogorski et al., 2006). An autosomal recessive form of monilethrix-like congenital hypotrichosis (see 607903) is caused by mutation in the DSG4 gene (607892). The clinical picture of autosomal recessive monilethrix is more severe than the dominant form, with more extensive alopecia of the scalp, body, and limbs, and a papular rash involving the extremities and periumbilical region (Zlotogorski et al., 2006). The term monilethrix derives from the Latin word for necklace and the Greek for hair (Schweizer, 2006).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/108185">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_272036"><div><strong>Trichothiodystrophy 4, nonphotosensitive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>272036</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.">C1313961</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Trichothiodystrophy is a rare autosomal recessive disorder in which patients have brittle, sulfur-deficient hair that displays a diagnostic alternating light and dark banding pattern, called 'tiger tail banding,' under polarizing microscopy. TTD patients display a wide variety of clinical features, including cutaneous, neurologic, and growth abnormalities. Common additional clinical features are ichthyosis, intellectual/developmental disabilities, decreased fertility, abnormal characteristics at birth, ocular abnormalities, short stature, and infections. There are both photosensitive and nonphotosensitive forms of the disorder (summary by Faghri et al., 2008). Sabinas brittle hair syndrome (211390) is another form of nonphotosensitive TTD. For a discussion of genetic heterogeneity of trichothiodystrophy, see 601675.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/272036">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_355853"><div><strong>Koolen-de Vries syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>355853</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:">C1864871</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Koolen-de Vries syndrome (KdVS) is characterized by congenital malformations, developmental delay / intellectual disability, neonatal/childhood hypotonia, epilepsy, dysmorphisms, and behavioral features. Psychomotor developmental delay is noted in all individuals from an early age. The majority of individuals with KdVS function in the mild-to-moderate range of intellectual disability. Other findings include speech and language delay (100%), epilepsy (~33%), congenital heart defects (25%-50%), renal and urologic anomalies (25%-50%), and cryptorchidism. Behavior in most is described as friendly, amiable, and cooperative.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/355853">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_400891"><div><strong>Odonto-tricho-ungual-digito-palmar syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>400891</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.">C1865998</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">This syndrome has characteristics of neonatal teeth, trichodystrophy and malformations of the hands and feet. To date, it has been reported in 21 patients and is transmitted as an autosomal dominant trait.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/400891">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_108185" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Beaded hair</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_82795" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cutis laxa with osteodystrophy</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_355853" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Koolen-de Vries syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_400891" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Odonto-tricho-ungual-digito-palmar syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_272036" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Trichothiodystrophy 4, nonphotosensitive</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/38447098">Keratosis pilaris treatment paradigms: assessing effectiveness across modalities.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wong PC,
|
||
Wang MA,
|
||
Ng TJ,
|
||
Akbarialiabad H,
|
||
Murrell DF</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Dermatol</span>
|
||
2024 Sep 18;49(10):1105-1117.
|
||
doi: 10.1093/ced/llae066.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38447098" target="_blank">38447098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20866114">Laser treatment of dark skin: an updated review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shah S,
|
||
Alster TS</span><br />
|
||
<span class="medgenPMjournal">Am J Clin Dermatol</span>
|
||
2010 Dec 1;11(6):389-97.
|
||
doi: 10.2165/11538940-000000000-00000.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20866114" target="_blank">20866114</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormality%20of%20hair%20texture)%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 (2)</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/39419623">Real-world safety profile of zanubrutinib: a disproportionality analysis based on the FAERS database.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang J,
|
||
Zheng X,
|
||
Lin J,
|
||
Huang J,
|
||
Zhang M,
|
||
Huang P,
|
||
Yang X</span><br />
|
||
<span class="medgenPMjournal">BMJ Open</span>
|
||
2024 Oct 17;14(10):e084991.
|
||
doi: 10.1136/bmjopen-2024-084991.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39419623" target="_blank">39419623</a><a href="/pmc/articles/PMC11487851" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36173944">Ultrathin Supratrochlear Artery Cutaneous Branch Flaps for Large Defects Around Eyebrows.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu Y,
|
||
Dai X,
|
||
Li N,
|
||
Lv T,
|
||
Che D,
|
||
Han J,
|
||
Dai Y,
|
||
Xiao Z</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2023 Mar-Apr 01;34(2):751-754.
|
||
Epub 2022 Sep 29
|
||
doi: 10.1097/SCS.0000000000009027.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36173944" target="_blank">36173944</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35178760">Follicular keratosis of the face in pediatric patients of color.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Grullon K,
|
||
Ashi SA,
|
||
Shea CR,
|
||
Ruiz de Luzuriaga AM,
|
||
Stein SL,
|
||
Rosenblatt AE</span><br />
|
||
<span class="medgenPMjournal">Pediatr Dermatol</span>
|
||
2022 Mar;39(2):231-235.
|
||
Epub 2022 Feb 17
|
||
doi: 10.1111/pde.14946.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35178760" target="_blank">35178760</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32944881">Prospective observational study of chemotherapy-induced alopecia after sequential FEC + taxane and the effects of age in breast cancer patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fujii T,
|
||
Ichiba K,
|
||
Honda C,
|
||
Tokuda S,
|
||
Nakazawa Y,
|
||
Ogino M,
|
||
Kurozumi S,
|
||
Obayashi S,
|
||
Yajima R,
|
||
Shirabe K</span><br />
|
||
<span class="medgenPMjournal">Breast Cancer</span>
|
||
2021 Mar;28(2):329-334.
|
||
Epub 2020 Sep 17
|
||
doi: 10.1007/s12282-020-01161-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32944881" target="_blank">32944881</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20866114">Laser treatment of dark skin: an updated review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shah S,
|
||
Alster TS</span><br />
|
||
<span class="medgenPMjournal">Am J Clin Dermatol</span>
|
||
2010 Dec 1;11(6):389-97.
|
||
doi: 10.2165/11538940-000000000-00000.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20866114" target="_blank">20866114</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20hair%20texture%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 (13)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38447098">Keratosis pilaris treatment paradigms: assessing effectiveness across modalities.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wong PC,
|
||
Wang MA,
|
||
Ng TJ,
|
||
Akbarialiabad H,
|
||
Murrell DF</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Dermatol</span>
|
||
2024 Sep 18;49(10):1105-1117.
|
||
doi: 10.1093/ced/llae066.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38447098" target="_blank">38447098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35751533">Uncombable hair syndrome and beyond.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alsabbagh MM</span><br />
|
||
<span class="medgenPMjournal">Acta Dermatovenerol Alp Pannonica Adriat</span>
|
||
2022 Jun;31(2):49-64.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35751533" target="_blank">35751533</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31736117">Comparison of hair manifestations in cardio-facio-cutaneous and Costello syndromes highlights the influence of the RAS pathway on hair growth.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Urban J,
|
||
Qi L,
|
||
Zhao H,
|
||
Rybak I,
|
||
Rauen KA,
|
||
Kiuru M</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2020 Mar;34(3):601-607.
|
||
Epub 2020 Jan 2
|
||
doi: 10.1111/jdv.16082.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31736117" target="_blank">31736117</a><a href="/pmc/articles/PMC7050334" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26858134">Dermatologic findings of focal dermal hypoplasia (Goltz syndrome).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bree AF,
|
||
Grange DK,
|
||
Hicks MJ,
|
||
Goltz RW</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet C Semin Med Genet</span>
|
||
2016 Mar;172C(1):44-51.
|
||
Epub 2016 Feb 9
|
||
doi: 10.1002/ajmg.c.31472.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26858134" target="_blank">26858134</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21182495">A practical, algorithmic approach to diagnosing hair shaft disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mirmirani P,
|
||
Huang KP,
|
||
Price VH</span><br />
|
||
<span class="medgenPMjournal">Int J Dermatol</span>
|
||
2011 Jan;50(1):1-12.
|
||
doi: 10.1111/j.1365-4632.2010.04768.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21182495" target="_blank">21182495</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20hair%20texture%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 (12)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39419623">Real-world safety profile of zanubrutinib: a disproportionality analysis based on the FAERS database.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang J,
|
||
Zheng X,
|
||
Lin J,
|
||
Huang J,
|
||
Zhang M,
|
||
Huang P,
|
||
Yang X</span><br />
|
||
<span class="medgenPMjournal">BMJ Open</span>
|
||
2024 Oct 17;14(10):e084991.
|
||
doi: 10.1136/bmjopen-2024-084991.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39419623" target="_blank">39419623</a><a href="/pmc/articles/PMC11487851" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38693620">Targeted therapies in ameloblastomas and amelobastic carcinoma-A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bologna-Molina R,
|
||
Schuch L,
|
||
Magliocca K,
|
||
van Heerden W,
|
||
Robinson L,
|
||
Bilodeau EA,
|
||
Hussaini HM,
|
||
Soluk-Tekkesin M,
|
||
Adisa AO,
|
||
Tilakaratne WM,
|
||
Li J,
|
||
Gomez RS,
|
||
Hunter KD</span><br />
|
||
<span class="medgenPMjournal">Oral Dis</span>
|
||
2024 Sep;30(6):3571-3581.
|
||
Epub 2024 May 1
|
||
doi: 10.1111/odi.14962.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38693620" target="_blank">38693620</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38447098">Keratosis pilaris treatment paradigms: assessing effectiveness across modalities.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wong PC,
|
||
Wang MA,
|
||
Ng TJ,
|
||
Akbarialiabad H,
|
||
Murrell DF</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Dermatol</span>
|
||
2024 Sep 18;49(10):1105-1117.
|
||
doi: 10.1093/ced/llae066.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38447098" target="_blank">38447098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26982511">Hair and Nail Changes During Long-term Therapy With Ibrutinib for Chronic Lymphocytic Leukemia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bitar C,
|
||
Farooqui MZ,
|
||
Valdez J,
|
||
Saba NS,
|
||
Soto S,
|
||
Bray A,
|
||
Marti G,
|
||
Wiestner A,
|
||
Cowen EW</span><br />
|
||
<span class="medgenPMjournal">JAMA Dermatol</span>
|
||
2016 Jun 1;152(6):698-701.
|
||
doi: 10.1001/jamadermatol.2016.0225.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26982511" target="_blank">26982511</a><a href="/pmc/articles/PMC6415534" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18004288">Healthy hair: what is it?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sinclair RD</span><br />
|
||
<span class="medgenPMjournal">J Investig Dermatol Symp Proc</span>
|
||
2007 Dec;12(2):2-5.
|
||
doi: 10.1038/sj.jidsymp.5650046.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18004288" target="_blank">18004288</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20hair%20texture%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 (15)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38693620">Targeted therapies in ameloblastomas and amelobastic carcinoma-A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bologna-Molina R,
|
||
Schuch L,
|
||
Magliocca K,
|
||
van Heerden W,
|
||
Robinson L,
|
||
Bilodeau EA,
|
||
Hussaini HM,
|
||
Soluk-Tekkesin M,
|
||
Adisa AO,
|
||
Tilakaratne WM,
|
||
Li J,
|
||
Gomez RS,
|
||
Hunter KD</span><br />
|
||
<span class="medgenPMjournal">Oral Dis</span>
|
||
2024 Sep;30(6):3571-3581.
|
||
Epub 2024 May 1
|
||
doi: 10.1111/odi.14962.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38693620" target="_blank">38693620</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36689522">Biallelic TUFT1 variants cause woolly hair, superficial skin fragility and desmosomal defects.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jackson A,
|
||
Moss C,
|
||
Chandler KE,
|
||
Balboa PL,
|
||
Bageta ML,
|
||
Petrof G,
|
||
Martinez AE,
|
||
Liu L,
|
||
Guy A,
|
||
Mellerio JE,
|
||
Lee JYW,
|
||
Ogboli M,
|
||
Ryan G;
|
||
Genomics England Research Consortium,
|
||
McGrath JA,
|
||
Banka S</span><br />
|
||
<span class="medgenPMjournal">Br J Dermatol</span>
|
||
2023 Jan 23;188(1):75-83.
|
||
doi: 10.1093/bjd/ljac026.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36689522" target="_blank">36689522</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26858134">Dermatologic findings of focal dermal hypoplasia (Goltz syndrome).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bree AF,
|
||
Grange DK,
|
||
Hicks MJ,
|
||
Goltz RW</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet C Semin Med Genet</span>
|
||
2016 Mar;172C(1):44-51.
|
||
Epub 2016 Feb 9
|
||
doi: 10.1002/ajmg.c.31472.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26858134" target="_blank">26858134</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25372313">Treatment of keratosis pilaris with 810-nm diode laser: a randomized clinical trial.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ibrahim O,
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Khan M,
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||
Bolotin D,
|
||
Dubina M,
|
||
Nodzenski M,
|
||
Disphanurat W,
|
||
Kakar R,
|
||
Yoo S,
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Whiting D,
|
||
West DP,
|
||
Poon E,
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||
Veledar E,
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||
Alam M</span><br />
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||
<span class="medgenPMjournal">JAMA Dermatol</span>
|
||
2015 Feb;151(2):187-91.
|
||
doi: 10.1001/jamadermatol.2014.2211.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25372313" target="_blank">25372313</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19659987">Repigmentation and curling of hair after acitretin therapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Seckin D,
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||
Yildiz A</span><br />
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||
<span class="medgenPMjournal">Australas J Dermatol</span>
|
||
2009 Aug;50(3):214-6.
|
||
doi: 10.1111/j.1440-0960.2009.00542.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19659987" target="_blank">19659987</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20hair%20texture%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 (10)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39419623">Real-world safety profile of zanubrutinib: a disproportionality analysis based on the FAERS database.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang J,
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Zheng X,
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||
Lin J,
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||
Huang J,
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||
Zhang M,
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||
Huang P,
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||
Yang X</span><br />
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||
<span class="medgenPMjournal">BMJ Open</span>
|
||
2024 Oct 17;14(10):e084991.
|
||
doi: 10.1136/bmjopen-2024-084991.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39419623" target="_blank">39419623</a><a href="/pmc/articles/PMC11487851" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38447098">Keratosis pilaris treatment paradigms: assessing effectiveness across modalities.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wong PC,
|
||
Wang MA,
|
||
Ng TJ,
|
||
Akbarialiabad H,
|
||
Murrell DF</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Dermatol</span>
|
||
2024 Sep 18;49(10):1105-1117.
|
||
doi: 10.1093/ced/llae066.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38447098" target="_blank">38447098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36689522">Biallelic TUFT1 variants cause woolly hair, superficial skin fragility and desmosomal defects.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jackson A,
|
||
Moss C,
|
||
Chandler KE,
|
||
Balboa PL,
|
||
Bageta ML,
|
||
Petrof G,
|
||
Martinez AE,
|
||
Liu L,
|
||
Guy A,
|
||
Mellerio JE,
|
||
Lee JYW,
|
||
Ogboli M,
|
||
Ryan G;
|
||
Genomics England Research Consortium,
|
||
McGrath JA,
|
||
Banka S</span><br />
|
||
<span class="medgenPMjournal">Br J Dermatol</span>
|
||
2023 Jan 23;188(1):75-83.
|
||
doi: 10.1093/bjd/ljac026.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36689522" target="_blank">36689522</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35751533">Uncombable hair syndrome and beyond.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alsabbagh MM</span><br />
|
||
<span class="medgenPMjournal">Acta Dermatovenerol Alp Pannonica Adriat</span>
|
||
2022 Jun;31(2):49-64.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35751533" target="_blank">35751533</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32944881">Prospective observational study of chemotherapy-induced alopecia after sequential FEC + taxane and the effects of age in breast cancer patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fujii T,
|
||
Ichiba K,
|
||
Honda C,
|
||
Tokuda S,
|
||
Nakazawa Y,
|
||
Ogino M,
|
||
Kurozumi S,
|
||
Obayashi S,
|
||
Yajima R,
|
||
Shirabe K</span><br />
|
||
<span class="medgenPMjournal">Breast Cancer</span>
|
||
2021 Mar;28(2):329-334.
|
||
Epub 2020 Sep 17
|
||
doi: 10.1007/s12282-020-01161-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32944881" target="_blank">32944881</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20hair%20texture%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 (13)</a></div></div>
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|
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<div class="nl"><a target="_blank" href="/pubmed/38693620">Targeted therapies in ameloblastomas and amelobastic carcinoma-A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bologna-Molina R,
|
||
Schuch L,
|
||
Magliocca K,
|
||
van Heerden W,
|
||
Robinson L,
|
||
Bilodeau EA,
|
||
Hussaini HM,
|
||
Soluk-Tekkesin M,
|
||
Adisa AO,
|
||
Tilakaratne WM,
|
||
Li J,
|
||
Gomez RS,
|
||
Hunter KD</span><br />
|
||
<span class="medgenPMjournal">Oral Dis</span>
|
||
2024 Sep;30(6):3571-3581.
|
||
Epub 2024 May 1
|
||
doi: 10.1111/odi.14962.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38693620" target="_blank">38693620</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14695500">Scalp hair characteristics in the newborn infant.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Furdon SA,
|
||
Clark DA</span><br />
|
||
<span class="medgenPMjournal">Adv Neonatal Care</span>
|
||
2003 Dec;3(6):286-96.
|
||
doi: 10.1016/j.adnc.2003.09.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14695500" target="_blank">14695500</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20hair%20texture%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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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormality%20of%20hair%20texture)%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(%22Abnormality%20of%20hair%20texture%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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