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<meta name="keywords" content="C4024297, abnormality of the hairline, anatomical abnormality, 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="The hairline refers to the outline of hair of the head. An abnormality of the hairline can refer to an unusually low or high border between areas of the scalp with and without hair or to abnormal projections of scalp hair." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=869866
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ConceptID=C4024297
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormality of the hairline</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>869866</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.">C4024297</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><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:0009553">HP:0009553</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">The hairline refers to the outline of hair of the head. An abnormality of the hairline can refer to an unusually low or high border between areas of the scalp with and without hair or to abnormal projections of scalp 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 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="TLline">Abnormality of the hairline</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/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/871249" ref="tree=MeSH" title="MedGen record for Abnormal scalp morphology">Abnormal scalp morphology</a></span><ul><li><span class="TLline"><a href="/medgen/867993" ref="tree=MeSH" title="MedGen record for Abnormality of the scalp hair">Abnormality of the scalp hair</a></span><ul><li><span class="matched_ds">Abnormality of the hairline</span><ul><li><span class="TLline"><a href="/medgen/871346" ref="tree=MeSH" title="MedGen record for Abnormality of the frontal hairline">Abnormality of the frontal hairline</a></span><ul><li><span class="TLline"><a href="/medgen/346590" ref="tree=MeSH" title="MedGen record for Extension of hair growth on temples to lateral eyebrow">Extension of hair growth on temples to lateral eyebrow</a></span></li><li><span class="TLline"><a href="/medgen/477667" ref="tree=MeSH" title="MedGen record for High anterior hairline">High anterior hairline</a></span><ul><li><span class="TLline"><a href="/medgen/342891" ref="tree=MeSH" title="MedGen record for Widow peak">Widow peak</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/331280" ref="tree=MeSH" title="MedGen record for Low anterior hairline">Low anterior hairline</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/868215" ref="tree=MeSH" title="MedGen record for Abnormality of the posterior hairline">Abnormality of the posterior hairline</a></span><ul><li><span class="TLline"><a href="/medgen/868298" ref="tree=MeSH" title="MedGen record for High posterior hairline">High posterior hairline</a></span></li><li><span class="TLline"><a href="/medgen/383755" ref="tree=MeSH" title="MedGen record for Low posterior hairline">Low posterior hairline</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/869865" ref="tree=MeSH" title="MedGen record for Preauricular hair displacement">Preauricular hair displacement</a></span></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_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_334629"><div><strong>Chromosome 1p36 deletion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>334629</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.">C1842870</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The constitutional deletion of chromosome 1p36 results in a syndrome with multiple congenital anomalies and mental retardation (Shapira et al., 1997). Monosomy 1p36 is the most common terminal deletion syndrome in humans, occurring in 1 in 5,000 births (Shaffer and Lupski, 2000; Heilstedt et al., 2003). See also neurodevelopmental disorder with or without anomalies of the brain, eye, or heart (NEDBEH; 616975), which shows overlapping features and is caused by heterozygous mutation in the RERE gene (605226) on proximal chromosome 1p36. See also Radio-Tartaglia syndrome (RATARS; 619312), caused by mutation in the SPEN gene (613484) on chromosome 1p36, which shows overlapping features.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/334629">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_383680"><div><strong>Oculotrichoanal syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>383680</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.">C1855425</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">FREM1 autosomal recessive disorders include Manitoba oculotrichoanal (MOTA) syndrome, bifid nose with or without anorectal and renal anomalies (BNAR syndrome), and isolated congenital anomalies of kidney and urinary tract (CAKUT). MOTA syndrome is characterized by an aberrant hairline (unilateral or bilateral wedge-shaped extension of the anterior hairline from the temple region to the ipsilateral eye) and anomalies of the eyes (widely spaced eyes, anophthalmia/microphthalmia and/or cryptophthalmos, colobomas of the upper eyelid, and corneopalpebral synechiae), nose (bifid or broad nasal tip), abdominal wall (omphalocele or umbilical hernia), and anus (stenosis and/or anterior displacement of the anal opening). The manifestations and degree of severity vary even among affected members of the same family. Growth and psychomotor development are normal. BNAR syndrome is characterized by a bifid or wide nasal tip, anorectal anomalies, and renal malformations (e.g., renal agenesis, renal dysplasia). Typically the eye manifestations of MOTA syndrome are absent. FREM1-CAKUT was identified in one individual with bilateral vesicoureteral reflux (VUR) and a second individual with VUR and renal hypodysplasia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/383680">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_350477"><div><strong>Rubinstein-Taybi syndrome due to 16p13.3 microdeletion</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>350477</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.">C1864648</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Chromosome 16p13.3deletion syndrome is a chromosome abnormality that can affect many parts of the body. People with this condition are missing a small piece (deletion) of chromosome 16 at a location designated p13.3. Although once thought to be a severe form of Rubinstein-Taybi syndrome, it is now emerging as a unique syndrome. Signs and symptoms may include failure to thrive, hypotonia (reduced muscle tone), short stature, microcephaly (unusually small head), characteristic facial features, mild to moderate intellectual disability, organ anomalies (i.e. heart and/or kidney problems), and vulnerability to infections. Chromosome testing of both parents can provide information about whether the deletion was inherited. In most cases, parents do not have any chromosome abnormalities. However, sometimes one parent has a balanced translocation where a piece of a chromosome has broken off and attached to another one with no gain or loss of genetic material. The balanced translocation normally does not cause signs or symptoms, but it increases the risk for having a child with a chromosome abnormality like a deletion. Treatment is based on the signs and symptoms present in each person.To learn more about chromosome abnormalities in general, view our GARD fact sheet on Chromosome Disorders.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/350477">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766916"><div><strong>Peroxisome biogenesis disorder 12A (Zellweger)</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766916</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.">C3554002</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Zellweger syndrome (ZS) is an autosomal recessive multiple congenital anomaly syndrome resulting from disordered peroxisome biogenesis. Affected children present in the newborn period with profound hypotonia, seizures, and inability to feed. Characteristic craniofacial anomalies, eye abnormalities, neuronal migration defects, hepatomegaly, and chondrodysplasia punctata are present. Children with this condition do not show any significant development and usually die in the first year of life (summary by Steinberg et al., 2006). For a complete phenotypic description and a discussion of genetic heterogeneity of Zellweger syndrome, see 214100. Individuals with PBDs of complementation group 14 (CG14, equivalent to CGJ) have mutations in the PEX19 gene. For information on the history of PBD complementation groups, see 214100.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766916">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_334629" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chromosome 1p36 deletion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_383680" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Oculotrichoanal syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766916" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Peroxisome biogenesis disorder 12A (Zellweger)</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_350477" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Rubinstein-Taybi syndrome due to 16p13.3 microdeletion</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/34628444">Turner syndrome mosaicism: Challenges in identification and management in primary care.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bryant PH,
|
||
Jacoby D,
|
||
Bunch M,
|
||
Speck PM</span><br />
|
||
<span class="medgenPMjournal">J Am Assoc Nurse Pract</span>
|
||
2021 Oct 7;34(2):400-404.
|
||
doi: 10.1097/JXX.0000000000000643.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34628444" target="_blank">34628444</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31677111">Female Androgenetic Alopecia: An Update on Diagnosis and Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Starace M,
|
||
Orlando G,
|
||
Alessandrini A,
|
||
Piraccini BM</span><br />
|
||
<span class="medgenPMjournal">Am J Clin Dermatol</span>
|
||
2020 Feb;21(1):69-84.
|
||
doi: 10.1007/s40257-019-00479-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31677111" target="_blank">31677111</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26509855">AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS, AMERICAN COLLEGE OF ENDOCRINOLOGY, AND ANDROGEN EXCESS AND PCOS SOCIETY DISEASE STATE CLINICAL REVIEW: GUIDE TO THE BEST PRACTICES IN THE EVALUATION AND TREATMENT OF POLYCYSTIC OVARY SYNDROME--PART 1.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goodman NF,
|
||
Cobin RH,
|
||
Futterweit W,
|
||
Glueck JS,
|
||
Legro RS,
|
||
Carmina E;
|
||
American Association of Clinical Endocrinologists (AACE);
|
||
American College of Endocrinology (ACE);
|
||
Androgen Excess and PCOS Society (AES)</span><br />
|
||
<span class="medgenPMjournal">Endocr Pract</span>
|
||
2015 Nov;21(11):1291-300.
|
||
doi: 10.4158/EP15748.DSC.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26509855" target="_blank">26509855</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormality%20of%20the%20hairline)%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 (6)</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/36716002">Above-The-Hairline Suboccipital Transverse Approach for the Treatment of Chiari I Malformation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Naylor RM,
|
||
Rotter J,
|
||
Proctor MR,
|
||
Bite U,
|
||
Ahn ES</span><br />
|
||
<span class="medgenPMjournal">Oper Neurosurg (Hagerstown)</span>
|
||
2023 May 1;24(5):542-547.
|
||
Epub 2023 Jan 19
|
||
doi: 10.1227/ons.0000000000000619.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36716002" target="_blank">36716002</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31854143">Turner syndrome in diverse populations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kruszka P,
|
||
Addissie YA,
|
||
Tekendo-Ngongang C,
|
||
Jones KL,
|
||
Savage SK,
|
||
Gupta N,
|
||
Sirisena ND,
|
||
Dissanayake VHW,
|
||
Paththinige CS,
|
||
Aravena T,
|
||
Nampoothiri S,
|
||
Yesodharan D,
|
||
Girisha KM,
|
||
Patil SJ,
|
||
Jamuar SS,
|
||
Goh JC,
|
||
Utari A,
|
||
Sihombing N,
|
||
Mishra R,
|
||
Chitrakar NS,
|
||
Iriele BC,
|
||
Lulseged E,
|
||
Megarbane A,
|
||
Uwineza A,
|
||
Oyenusi EE,
|
||
Olopade OB,
|
||
Fasanmade OA,
|
||
Duenas-Roque MM,
|
||
Thong MK,
|
||
Tung JYL,
|
||
Mok GTK,
|
||
Fleischer N,
|
||
Rwegerera GM,
|
||
de Herreros MB,
|
||
Watts J,
|
||
Fieggen K,
|
||
Huckstadt V,
|
||
Moresco A,
|
||
Obregon MG,
|
||
Hussen DF,
|
||
Ashaat NA,
|
||
Ashaat EA,
|
||
Chung BHY,
|
||
Badoe E,
|
||
Faradz SMH,
|
||
El Ruby MO,
|
||
Shotelersuk V,
|
||
Wonkam A,
|
||
Ekure EN,
|
||
Phadke SR,
|
||
Richieri-Costa A,
|
||
Muenke M</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2020 Feb;182(2):303-313.
|
||
Epub 2019 Dec 19
|
||
doi: 10.1002/ajmg.a.61461.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31854143" target="_blank">31854143</a><a href="/pmc/articles/PMC8141514" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29886918">The Prevalence of Klippel-Feil Syndrome: A Computed Tomography-Based Analysis of 2,917 Patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gruber J,
|
||
Saleh A,
|
||
Bakhsh W,
|
||
Rubery PT,
|
||
Mesfin A</span><br />
|
||
<span class="medgenPMjournal">Spine Deform</span>
|
||
2018 Jul-Aug;6(4):448-453.
|
||
doi: 10.1016/j.jspd.2017.12.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29886918" target="_blank">29886918</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26509855">AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS, AMERICAN COLLEGE OF ENDOCRINOLOGY, AND ANDROGEN EXCESS AND PCOS SOCIETY DISEASE STATE CLINICAL REVIEW: GUIDE TO THE BEST PRACTICES IN THE EVALUATION AND TREATMENT OF POLYCYSTIC OVARY SYNDROME--PART 1.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goodman NF,
|
||
Cobin RH,
|
||
Futterweit W,
|
||
Glueck JS,
|
||
Legro RS,
|
||
Carmina E;
|
||
American Association of Clinical Endocrinologists (AACE);
|
||
American College of Endocrinology (ACE);
|
||
Androgen Excess and PCOS Society (AES)</span><br />
|
||
<span class="medgenPMjournal">Endocr Pract</span>
|
||
2015 Nov;21(11):1291-300.
|
||
doi: 10.4158/EP15748.DSC.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26509855" target="_blank">26509855</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22216833">Chromosome 15q24 microdeletion syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Magoulas PL,
|
||
El-Hattab AW</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2012 Jan 4;7:2.
|
||
doi: 10.1186/1750-1172-7-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22216833" target="_blank">22216833</a><a href="/pmc/articles/PMC3275445" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20hairline%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 (48)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31677111">Female Androgenetic Alopecia: An Update on Diagnosis and Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Starace M,
|
||
Orlando G,
|
||
Alessandrini A,
|
||
Piraccini BM</span><br />
|
||
<span class="medgenPMjournal">Am J Clin Dermatol</span>
|
||
2020 Feb;21(1):69-84.
|
||
doi: 10.1007/s40257-019-00479-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31677111" target="_blank">31677111</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30381133">A Slowly Receding Hairline.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Koushk-Jalali B,
|
||
Tigges C,
|
||
Kreuter A</span><br />
|
||
<span class="medgenPMjournal">Dtsch Arztebl Int</span>
|
||
2018 Nov 5;115(40):673.
|
||
doi: 10.3238/arztebl.2018.0673.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30381133" target="_blank">30381133</a><a href="/pmc/articles/PMC6234469" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26509855">AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS, AMERICAN COLLEGE OF ENDOCRINOLOGY, AND ANDROGEN EXCESS AND PCOS SOCIETY DISEASE STATE CLINICAL REVIEW: GUIDE TO THE BEST PRACTICES IN THE EVALUATION AND TREATMENT OF POLYCYSTIC OVARY SYNDROME--PART 1.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goodman NF,
|
||
Cobin RH,
|
||
Futterweit W,
|
||
Glueck JS,
|
||
Legro RS,
|
||
Carmina E;
|
||
American Association of Clinical Endocrinologists (AACE);
|
||
American College of Endocrinology (ACE);
|
||
Androgen Excess and PCOS Society (AES)</span><br />
|
||
<span class="medgenPMjournal">Endocr Pract</span>
|
||
2015 Nov;21(11):1291-300.
|
||
doi: 10.4158/EP15748.DSC.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26509855" target="_blank">26509855</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24566563">Androgenetic alopecia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Piraccini BM,
|
||
Alessandrini A</span><br />
|
||
<span class="medgenPMjournal">G Ital Dermatol Venereol</span>
|
||
2014 Feb;149(1):15-24.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24566563" target="_blank">24566563</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1739048">Klippel-Feil syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McBride WZ</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
1992 Feb;45(2):633-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1739048" target="_blank">1739048</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20hairline%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 (136)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31677111">Female Androgenetic Alopecia: An Update on Diagnosis and Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Starace M,
|
||
Orlando G,
|
||
Alessandrini A,
|
||
Piraccini BM</span><br />
|
||
<span class="medgenPMjournal">Am J Clin Dermatol</span>
|
||
2020 Feb;21(1):69-84.
|
||
doi: 10.1007/s40257-019-00479-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31677111" target="_blank">31677111</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28509671">Complications in facial Mohs defect reconstruction.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Berens AM,
|
||
Akkina SR,
|
||
Patel SA</span><br />
|
||
<span class="medgenPMjournal">Curr Opin Otolaryngol Head Neck Surg</span>
|
||
2017 Aug;25(4):258-264.
|
||
doi: 10.1097/MOO.0000000000000375.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28509671" target="_blank">28509671</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26509855">AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS, AMERICAN COLLEGE OF ENDOCRINOLOGY, AND ANDROGEN EXCESS AND PCOS SOCIETY DISEASE STATE CLINICAL REVIEW: GUIDE TO THE BEST PRACTICES IN THE EVALUATION AND TREATMENT OF POLYCYSTIC OVARY SYNDROME--PART 1.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goodman NF,
|
||
Cobin RH,
|
||
Futterweit W,
|
||
Glueck JS,
|
||
Legro RS,
|
||
Carmina E;
|
||
American Association of Clinical Endocrinologists (AACE);
|
||
American College of Endocrinology (ACE);
|
||
Androgen Excess and PCOS Society (AES)</span><br />
|
||
<span class="medgenPMjournal">Endocr Pract</span>
|
||
2015 Nov;21(11):1291-300.
|
||
doi: 10.4158/EP15748.DSC.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26509855" target="_blank">26509855</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24566563">Androgenetic alopecia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Piraccini BM,
|
||
Alessandrini A</span><br />
|
||
<span class="medgenPMjournal">G Ital Dermatol Venereol</span>
|
||
2014 Feb;149(1):15-24.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24566563" target="_blank">24566563</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19341939">Hair loss in women.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Camacho-Martínez FM</span><br />
|
||
<span class="medgenPMjournal">Semin Cutan Med Surg</span>
|
||
2009 Mar;28(1):19-32.
|
||
doi: 10.1016/j.sder.2009.01.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19341939" target="_blank">19341939</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20hairline%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 (24)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38527346">Encephalocraniocutaneous Lipomatosis: A Case Report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zaworski E,
|
||
Gruber E,
|
||
Regent-Smith A,
|
||
Jones KL,
|
||
Chalhoub MS,
|
||
Lin K</span><br />
|
||
<span class="medgenPMjournal">Ann Plast Surg</span>
|
||
2024 Apr 1;92(4):e29-e31.
|
||
doi: 10.1097/SAP.0000000000003814.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38527346" target="_blank">38527346</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26509855">AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS, AMERICAN COLLEGE OF ENDOCRINOLOGY, AND ANDROGEN EXCESS AND PCOS SOCIETY DISEASE STATE CLINICAL REVIEW: GUIDE TO THE BEST PRACTICES IN THE EVALUATION AND TREATMENT OF POLYCYSTIC OVARY SYNDROME--PART 1.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goodman NF,
|
||
Cobin RH,
|
||
Futterweit W,
|
||
Glueck JS,
|
||
Legro RS,
|
||
Carmina E;
|
||
American Association of Clinical Endocrinologists (AACE);
|
||
American College of Endocrinology (ACE);
|
||
Androgen Excess and PCOS Society (AES)</span><br />
|
||
<span class="medgenPMjournal">Endocr Pract</span>
|
||
2015 Nov;21(11):1291-300.
|
||
doi: 10.4158/EP15748.DSC.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26509855" target="_blank">26509855</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24566563">Androgenetic alopecia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Piraccini BM,
|
||
Alessandrini A</span><br />
|
||
<span class="medgenPMjournal">G Ital Dermatol Venereol</span>
|
||
2014 Feb;149(1):15-24.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24566563" target="_blank">24566563</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22216833">Chromosome 15q24 microdeletion syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Magoulas PL,
|
||
El-Hattab AW</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2012 Jan 4;7:2.
|
||
doi: 10.1186/1750-1172-7-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22216833" target="_blank">22216833</a><a href="/pmc/articles/PMC3275445" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1739048">Klippel-Feil syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McBride WZ</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
1992 Feb;45(2):633-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1739048" target="_blank">1739048</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20hairline%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 (30)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37939916">Facial dysmorphism in congenital rubella syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chattannavar G,
|
||
Bansal A,
|
||
Kekunnaya R</span><br />
|
||
<span class="medgenPMjournal">J AAPOS</span>
|
||
2024 Feb;28(1):103791.
|
||
Epub 2023 Nov 7
|
||
doi: 10.1016/j.jaapos.2023.08.020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37939916" target="_blank">37939916</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35550183">From Wolf-Hirschhorn syndrome to NSD2 haploinsufficiency: a shifting paradigm through the description of a new case and a review of the literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wiel LC,
|
||
Bruno I,
|
||
Barbi E,
|
||
Sirchia F</span><br />
|
||
<span class="medgenPMjournal">Ital J Pediatr</span>
|
||
2022 May 12;48(1):72.
|
||
doi: 10.1186/s13052-022-01267-w.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35550183" target="_blank">35550183</a><a href="/pmc/articles/PMC9097050" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31179579">Frontal fibrosing alopecia: demographic and clinical characteristics of 490 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kanti V,
|
||
Constantinou A,
|
||
Reygagne P,
|
||
Vogt A,
|
||
Kottner J,
|
||
Blume-Peytavi U</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2019 Oct;33(10):1976-1983.
|
||
Epub 2019 Jul 1
|
||
doi: 10.1111/jdv.15735.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31179579" target="_blank">31179579</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26509855">AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS, AMERICAN COLLEGE OF ENDOCRINOLOGY, AND ANDROGEN EXCESS AND PCOS SOCIETY DISEASE STATE CLINICAL REVIEW: GUIDE TO THE BEST PRACTICES IN THE EVALUATION AND TREATMENT OF POLYCYSTIC OVARY SYNDROME--PART 1.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goodman NF,
|
||
Cobin RH,
|
||
Futterweit W,
|
||
Glueck JS,
|
||
Legro RS,
|
||
Carmina E;
|
||
American Association of Clinical Endocrinologists (AACE);
|
||
American College of Endocrinology (ACE);
|
||
Androgen Excess and PCOS Society (AES)</span><br />
|
||
<span class="medgenPMjournal">Endocr Pract</span>
|
||
2015 Nov;21(11):1291-300.
|
||
doi: 10.4158/EP15748.DSC.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26509855" target="_blank">26509855</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22216833">Chromosome 15q24 microdeletion syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Magoulas PL,
|
||
El-Hattab AW</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2012 Jan 4;7:2.
|
||
doi: 10.1186/1750-1172-7-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22216833" target="_blank">22216833</a><a href="/pmc/articles/PMC3275445" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20hairline%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 (38)</a></div></div>
|
||
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|
||
|
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|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/30785992">Female Pattern Hair Loss and Androgen Excess: A Report From the Multidisciplinary Androgen Excess and PCOS Committee.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carmina E,
|
||
Azziz R,
|
||
Bergfeld W,
|
||
Escobar-Morreale HF,
|
||
Futterweit W,
|
||
Huddleston H,
|
||
Lobo R,
|
||
Olsen E</span><br />
|
||
<span class="medgenPMjournal">J Clin Endocrinol Metab</span>
|
||
2019 Jul 1;104(7):2875-2891.
|
||
doi: 10.1210/jc.2018-02548.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30785992" target="_blank">30785992</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%20the%20hairline%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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|
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|
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|
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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%20the%20hairline)%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%20the%20hairline%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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