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<meta name="keywords" content="C1859391, absent pubic hair, finding, no pubic hair, 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="Absence of pubic hair." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=349155
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ConceptID=C1859391
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Absent pubic hair</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>349155</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:">C1859391</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
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<td>No pubic hair</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:0002555">HP:0002555</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">Absence of pubic 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="TLline">Absent pubic hair</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="TLline"><a href="/medgen/869742" ref="tree=MeSH" title="MedGen record for Abnormality of secondary sexual hair">Abnormality of secondary sexual hair</a></span><ul><li><span class="TLline"><a href="/medgen/867897" ref="tree=MeSH" title="MedGen record for Abnormality of the pubic hair">Abnormality of the pubic hair</a></span><ul><li><span class="matched_ds">Absent pubic hair</span></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_56416"><div><strong>Hidrotic ectodermal dysplasia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>56416</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0162361</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hidrotic ectodermal dysplasia 2, or Clouston syndrome (referred to as HED2 throughout this GeneReview) is characterized by a triad of major clinical features including partial-to-complete alopecia, nail dystrophy, and palmoplantar hyperkeratosis. Sweating is preserved and there are usually no dental anomalies. Sparse scalp hair and dysplastic nails are seen early in life. In infancy, scalp hair is fine, sparse, and brittle. Progressive hair loss may lead to total alopecia by puberty. The nails may be milky white in early childhood; they gradually become dystrophic, thick, and distally separated from the nail bed. Palmoplantar keratoderma may develop during childhood and increases in severity with age. Associated features may include cutaneous hyperpigmentation (particularly over the joints) and finger clubbing. The clinical manifestations are highly variable even within the same family.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/56416">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_120536"><div><strong>Autosomal dominant keratitis-ichthyosis-hearing loss syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>120536</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.">C0265336</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Keratitis-ichthyosis-deafness (KID) syndrome is a rare ectodermal dysplasia characterized by sensorineural hearing loss, photophobia and corneal vascularization, hyperkeratosis of the palms and soles, erythrokeratoderma, follicular hyperkeratosis, and recurrent bacterial and fungal infections. A subset of patients with KID may develop multiple cystic pilar tumors, which are prone to malignant transformation and metastasis (Nyquist et al., 2007). Vohwinkel syndrome (124500) is an allelic disorder involving congenital deafness with keratopachydermia and constrictions of fingers and toes. Another similar disorder caused by mutation in GJB2 is palmoplantar keratoderma with deafness (148350). Genetic Heterogeneity of Keratitis-Ichthyosis-Deafness Syndrome An autosomal recessive form of KID syndrome (KIDAR; 242150) is caused by mutation in the AP1B1 gene (600157) on chromosome 22q12.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/120536">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_347328"><div><strong>Hypogonadotropic hypogonadism 12 with or without anosmia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347328</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.">C1856897</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Isolated gonadotropin-releasing hormone (GnRH) deficiency (IGD) is characterized by inappropriately low serum concentrations of the gonadotropins LH (luteinizing hormone) and FSH (follicle-stimulating hormone) in the presence of low circulating concentrations of sex steroids. IGD is associated with a normal sense of smell (normosmic IGD) in approximately 40% of affected individuals and an impaired sense of smell (Kallmann syndrome) in approximately 60%. IGD can first become apparent in infancy, adolescence, or adulthood. Infant boys with congenital IGD often have micropenis and cryptorchidism. Adolescents and adults with IGD have clinical evidence of hypogonadism and incomplete sexual maturation on physical examination. Adult males with IGD tend to have prepubertal testicular volume (i.e., <4 mL), absence of secondary sexual features (e.g., facial and axillary hair growth, deepening of the voice), decreased muscle mass, diminished libido, erectile dysfunction, and infertility. Adult females have little or no breast development and primary amenorrhea. Although skeletal maturation is delayed, the rate of linear growth is usually normal except for the absence of a distinct pubertal growth spurt.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/347328">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_349262"><div><strong>Alopecia universalis congenita</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>349262</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.">C1859877</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Alopecia universalis congenita (ALUNC) is a severe autosomal recessive form of alopecia characterized by a complete absence of hair development affecting all scalp and body hair (Nothen et al., 1998). This rare disorder is clearly distinct from alopecia areata (AA1; 104000), which has an autoimmune basis with probable genetic predisposition.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/349262">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_440568"><div><strong>Hypotrichosis 5</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>440568</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.">C2748535</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypotrichosis-5 (HYPT5), also known as Marie Unna hereditary hypotrichosis-2 (MUHH2), is a form of hereditary hypotrichosis characterized by twisting hair. Affected individuals have little or no scalp hair at birth, wiry and irregular scalp hair in childhood, and sparse or no forehead and parietal hair at puberty. Eyebrows and eyelashes are thin, and pubic and axillary hair fails to develop. Scarring alopecia is modest, and vertex hair is normal (summary by Zhang et al., 2012). For a general phenotypic description of Marie Unna hereditary hypotrichosis, see MUHH1 (146550). For a discussion of genetic heterogeneity of nonsyndromic hypotrichosis, see 605389.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/440568">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_414115"><div><strong>Premature ovarian failure 7</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>414115</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.">C2751825</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any primary ovarian failure in which the cause of the disease is a mutation in the NR5A1 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/414115">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1811851"><div><strong>Epidermolysis bullosa, junctional 5A, intermediate</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1811851</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.">C5676956</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Intermediate junctional epidermolysis bullosa 5A (JEB5A) is an autosomal recessive blistering disease of skin and mucous membranes. Blistering is less severe than in severe JEB (see 226700). The plane of skin cleavage is through the lamina lucida of the cutaneous basement membrane zone. Nails may be dystrophic and dental enamel defects are present. Blistering does not affect the life span of affected individuals (summary by Has et al., 2020). For a discussion of genetic heterogeneity of the subtypes of JEB, see JEB1A (226650). Reviews Has et al. (2020) reviewed the clinical and genetic aspects, genotype-phenotype correlations, disease-modifying factors, and natural history of epidermolysis bullosa.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1811851">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_349262" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Alopecia universalis congenita</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_120536" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant keratitis-ichthyosis-hearing loss syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1811851" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Epidermolysis bullosa, junctional 5A, intermediate</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_56416" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hidrotic ectodermal dysplasia syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_347328" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypogonadotropic hypogonadism 12 with or without anosmia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_440568" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypotrichosis 5</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_414115" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Premature ovarian failure 7</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/11549642">Genotype versus phenotype in families with androgen insensitivity syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Boehmer AL,
|
||
Brinkmann O,
|
||
Brüggenwirth H,
|
||
van Assendelft C,
|
||
Otten BJ,
|
||
Verleun-Mooijman MC,
|
||
Niermeijer MF,
|
||
Brunner HG,
|
||
Rouwé CW,
|
||
Waelkens JJ,
|
||
Oostdijk W,
|
||
Kleijer WJ,
|
||
van der Kwast TH,
|
||
de Vroede MA,
|
||
Drop SL</span><br />
|
||
<span class="medgenPMjournal">J Clin Endocrinol Metab</span>
|
||
2001 Sep;86(9):4151-60.
|
||
doi: 10.1210/jcem.86.9.7825.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11549642" target="_blank">11549642</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(absent%20pubic%20hair)%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 (1)</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/34119661">Implications of Ehlers-Danlos Syndrome in a Patient With Mayer-Rokitansky-Küster-Hauser Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Brander EPA,
|
||
Dietrich JE</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Adolesc Gynecol</span>
|
||
2021 Dec;34(6):890-892.
|
||
Epub 2021 Jun 11
|
||
doi: 10.1016/j.jpag.2021.06.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34119661" target="_blank">34119661</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29462708">Diversity of Pubertal Development in Cartilage-Hair Hypoplasia; Two Illustrative Cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Holopainen E,
|
||
Vakkilainen S,
|
||
Mäkitie O</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Adolesc Gynecol</span>
|
||
2018 Aug;31(4):422-425.
|
||
Epub 2018 Feb 17
|
||
doi: 10.1016/j.jpag.2018.02.128.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29462708" target="_blank">29462708</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27594153">Clinical Features of 32 Patients with XO/XY Gonadal Dysgenesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jiang JF,
|
||
Tian QJ,
|
||
Xue W,
|
||
Deng Y,
|
||
Zheng TP,
|
||
Sun AJ</span><br />
|
||
<span class="medgenPMjournal">Zhongguo Yi Xue Ke Xue Yuan Xue Bao</span>
|
||
2016 Aug;38(4):411-4.
|
||
doi: 10.3881/j.issn.1000-503X.2016.04.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27594153" target="_blank">27594153</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24333107">Complete androgen insensitivity syndrome with a Sertoli-Leydig cell tumor.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fagouri H,
|
||
Moussaoui DR,
|
||
Kouach J,
|
||
Babahabib A,
|
||
Oukabli M,
|
||
Ameur A,
|
||
Albouzidi A,
|
||
Dehayni M</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Adolesc Gynecol</span>
|
||
2014 Oct;27(5):e113-5.
|
||
Epub 2013 Dec 14
|
||
doi: 10.1016/j.jpag.2013.08.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24333107" target="_blank">24333107</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6775000">The effects of exercise on pubertal progression and reproductive function in girls.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Warren MP</span><br />
|
||
<span class="medgenPMjournal">J Clin Endocrinol Metab</span>
|
||
1980 Nov;51(5):1150-7.
|
||
doi: 10.1210/jcem-51-5-1150.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6775000" target="_blank">6775000</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Absent%20pubic%20hair%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/34488834">Delayed pubarche.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baldo F,
|
||
Barbi E,
|
||
Tornese G</span><br />
|
||
<span class="medgenPMjournal">Ital J Pediatr</span>
|
||
2021 Sep 6;47(1):180.
|
||
doi: 10.1186/s13052-021-01134-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34488834" target="_blank">34488834</a><a href="/pmc/articles/PMC8422600" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24333107">Complete androgen insensitivity syndrome with a Sertoli-Leydig cell tumor.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fagouri H,
|
||
Moussaoui DR,
|
||
Kouach J,
|
||
Babahabib A,
|
||
Oukabli M,
|
||
Ameur A,
|
||
Albouzidi A,
|
||
Dehayni M</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Adolesc Gynecol</span>
|
||
2014 Oct;27(5):e113-5.
|
||
Epub 2013 Dec 14
|
||
doi: 10.1016/j.jpag.2013.08.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24333107" target="_blank">24333107</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23044874">Inactivating mutations of the human luteinizing hormone receptor in both sexes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Latronico AC,
|
||
Arnhold IJ</span><br />
|
||
<span class="medgenPMjournal">Semin Reprod Med</span>
|
||
2012 Oct;30(5):382-6.
|
||
Epub 2012 Oct 8
|
||
doi: 10.1055/s-0032-1324721.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23044874" target="_blank">23044874</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18590867">Premature adrenarche.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leung AK,
|
||
Robson WL</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Health Care</span>
|
||
2008 Jul-Aug;22(4):230-3.
|
||
Epub 2008 Mar 5
|
||
doi: 10.1016/j.pedhc.2007.07.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18590867" target="_blank">18590867</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17472679">Late-onset Rothmund-Thomson syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kumar P,
|
||
Sharma PK,
|
||
Gautam RK,
|
||
Jain RK,
|
||
Kar HK</span><br />
|
||
<span class="medgenPMjournal">Int J Dermatol</span>
|
||
2007 May;46(5):492-3.
|
||
doi: 10.1111/j.1365-4632.2007.03248.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17472679" target="_blank">17472679</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Absent%20pubic%20hair%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 (31)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36409615">Case 308: Van Wyk-Grumbach Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kandasamy D,
|
||
Malik R,
|
||
Sharma R,
|
||
Jana M</span><br />
|
||
<span class="medgenPMjournal">Radiology</span>
|
||
2022 Dec;305(3):746-750.
|
||
doi: 10.1148/radiol.211119.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36409615" target="_blank">36409615</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34488834">Delayed pubarche.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baldo F,
|
||
Barbi E,
|
||
Tornese G</span><br />
|
||
<span class="medgenPMjournal">Ital J Pediatr</span>
|
||
2021 Sep 6;47(1):180.
|
||
doi: 10.1186/s13052-021-01134-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34488834" target="_blank">34488834</a><a href="/pmc/articles/PMC8422600" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33096991">Massive pericardial effusion and cardiac tamponade revealed undiagnosed Turner syndrome: a case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Qiang W,
|
||
Sun R,
|
||
Zheng X,
|
||
Du Y</span><br />
|
||
<span class="medgenPMjournal">BMC Cardiovasc Disord</span>
|
||
2020 Oct 23;20(1):459.
|
||
doi: 10.1186/s12872-020-01728-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33096991" target="_blank">33096991</a><a href="/pmc/articles/PMC7583196" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29431100">Sheehan's syndrome presenting as cardiac tamponade.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mittal A,
|
||
Ray A,
|
||
Talupula RM,
|
||
Sood R</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2018 Feb 3;2018
|
||
doi: 10.1136/bcr-2017-223129.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29431100" target="_blank">29431100</a><a href="/pmc/articles/PMC5812377" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20841307">46, XX SRY-positive male syndrome presenting with primary hypogonadism in the setting of scleroderma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Velasco G,
|
||
Savarese V,
|
||
Sandorfi N,
|
||
Jimenez SA,
|
||
Jabbour S</span><br />
|
||
<span class="medgenPMjournal">Endocr Pract</span>
|
||
2011 Jan-Feb;17(1):95-8.
|
||
doi: 10.4158/EP10184.CR.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20841307" target="_blank">20841307</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Absent%20pubic%20hair%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 (7)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36409615">Case 308: Van Wyk-Grumbach Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kandasamy D,
|
||
Malik R,
|
||
Sharma R,
|
||
Jana M</span><br />
|
||
<span class="medgenPMjournal">Radiology</span>
|
||
2022 Dec;305(3):746-750.
|
||
doi: 10.1148/radiol.211119.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36409615" target="_blank">36409615</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35877547">Case 308.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kandasamy D,
|
||
Malik R,
|
||
Sharma R,
|
||
Jana M</span><br />
|
||
<span class="medgenPMjournal">Radiology</span>
|
||
2022 Aug;304(2):485-487.
|
||
doi: 10.1148/radiol.211118.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35877547" target="_blank">35877547</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20308033">Investigation of relationships between urinary biomarkers of phytoestrogens, phthalates, and phenols and pubertal stages in girls.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wolff MS,
|
||
Teitelbaum SL,
|
||
Pinney SM,
|
||
Windham G,
|
||
Liao L,
|
||
Biro F,
|
||
Kushi LH,
|
||
Erdmann C,
|
||
Hiatt RA,
|
||
Rybak ME,
|
||
Calafat AM;
|
||
Breast Cancer and Environment Research Centers</span><br />
|
||
<span class="medgenPMjournal">Environ Health Perspect</span>
|
||
2010 Jul;118(7):1039-46.
|
||
Epub 2010 Mar 22
|
||
doi: 10.1289/ehp.0901690.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20308033" target="_blank">20308033</a><a href="/pmc/articles/PMC2920905" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18422032">Novel mutation in cytochrome P450c17 causes complete combined 17alpha-hydroxylase/17,20-lyase deficiency.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bhangoo A,
|
||
Aisenberg J,
|
||
Chartoffe A,
|
||
Ten S,
|
||
Wallerstein RJ,
|
||
Wolf R,
|
||
Auchus RJ</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Endocrinol Metab</span>
|
||
2008 Feb;21(2):185-90.
|
||
doi: 10.1515/jpem.2008.21.2.185.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18422032" target="_blank">18422032</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Absent%20pubic%20hair%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 (4)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35443324">Different Cases of Short Stature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sathyanarayanan,
|
||
Ramkumar,
|
||
Dinesh S</span><br />
|
||
<span class="medgenPMjournal">J Assoc Physicians India</span>
|
||
2022 Apr;70(4):11-12.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35443324" target="_blank">35443324</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27594153">Clinical Features of 32 Patients with XO/XY Gonadal Dysgenesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jiang JF,
|
||
Tian QJ,
|
||
Xue W,
|
||
Deng Y,
|
||
Zheng TP,
|
||
Sun AJ</span><br />
|
||
<span class="medgenPMjournal">Zhongguo Yi Xue Ke Xue Yuan Xue Bao</span>
|
||
2016 Aug;38(4):411-4.
|
||
doi: 10.3881/j.issn.1000-503X.2016.04.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27594153" target="_blank">27594153</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18590867">Premature adrenarche.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leung AK,
|
||
Robson WL</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Health Care</span>
|
||
2008 Jul-Aug;22(4):230-3.
|
||
Epub 2008 Mar 5
|
||
doi: 10.1016/j.pedhc.2007.07.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18590867" target="_blank">18590867</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17472679">Late-onset Rothmund-Thomson syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kumar P,
|
||
Sharma PK,
|
||
Gautam RK,
|
||
Jain RK,
|
||
Kar HK</span><br />
|
||
<span class="medgenPMjournal">Int J Dermatol</span>
|
||
2007 May;46(5):492-3.
|
||
doi: 10.1111/j.1365-4632.2007.03248.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17472679" target="_blank">17472679</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16210857">Absent or delayed adrenarche in Pit-1/POU1F1 deficiency.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Taha D,
|
||
Mullis PE,
|
||
Ibáñez L,
|
||
de Zegher F</span><br />
|
||
<span class="medgenPMjournal">Horm Res</span>
|
||
2005;64(4):175-9.
|
||
Epub 2005 Oct 4
|
||
doi: 10.1159/000088793.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16210857" target="_blank">16210857</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Absent%20pubic%20hair%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 (15)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
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<div class="nl"><a target="_blank" href="/pubmed/31336995">46,XX Testicular Disorder of Sex Development (DSD): A Case Report and Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Terribile M,
|
||
Stizzo M,
|
||
Manfredi C,
|
||
Quattrone C,
|
||
Bottone F,
|
||
Giordano DR,
|
||
Bellastella G,
|
||
Arcaniolo D,
|
||
De Sio M</span><br />
|
||
<span class="medgenPMjournal">Medicina (Kaunas)</span>
|
||
2019 Jul 12;55(7)
|
||
doi: 10.3390/medicina55070371.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31336995" target="_blank">31336995</a><a href="/pmc/articles/PMC6681203" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Absent%20pubic%20hair%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 (1)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
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|
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|
||
|
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|
||
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|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
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|
||
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Absent%20pubic%20hair" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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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=(absent%20pubic%20hair)%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(%22Absent%20pubic%20hair%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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<a href="/pubmed/clinical?term=Absent%20pubic%20hair" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Absent%20pubic%20hair%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=349155" ref="log$=recordlinks">ClinVar</a>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67ce8afaa68b6b5afc2ad2f1">Absent pubic hair</a>
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