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<meta name="keywords" content="C4025901, abnormality of body height, finding, 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="Deviation from the norm of height with respect to that which is expected according to age and gender norms." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=871403
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ConceptID=C4025901
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormality of body height</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>871403</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:">C4025901</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</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:0000002">HP:0000002</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">Deviation from the norm of height with respect to that which is expected according to age and gender norms. [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 body height</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/808205" ref="tree=MeSH" title="MedGen record for Growth abnormality">Growth abnormality</a></span><ul><li><span class="matched_ds">Abnormality of body height</span><ul><li><span class="TLline"><a href="/medgen/868334" ref="tree=MeSH" title="MedGen record for Abnormal upper to lower segment ratio">Abnormal upper to lower segment ratio</a></span><ul><li><span class="TLline"><a href="/medgen/375459" ref="tree=MeSH" title="MedGen record for Increased upper to lower segment ratio">Increased upper to lower segment ratio</a></span></li><li><span class="TLline"><a href="/medgen/1632800" ref="tree=MeSH" title="MedGen record for Reduced upper to lower segment ratio">Reduced upper to lower segment ratio</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/69137" ref="tree=MeSH" title="MedGen record for Tall stature">Tall stature</a></span><ul><li><span class="TLline"><a href="/medgen/326443" ref="tree=MeSH" title="MedGen record for Birth length greater than 97th percentile">Birth length greater than 97th percentile</a></span></li><li><span class="TLline"><a href="/medgen/323048" ref="tree=MeSH" title="MedGen record for Disproportionate tall stature">Disproportionate tall stature</a></span></li><li><span class="TLline"><a href="/medgen/858407" ref="tree=MeSH" title="MedGen record for Idiopathic Tall Stature">Idiopathic Tall Stature</a></span><ul><li><span class="TLline"><a href="/medgen/858750" ref="tree=MeSH" title="MedGen record for Familial Idiopathic Tall Stature">Familial Idiopathic Tall Stature</a></span></li><li><span class="TLline"><a href="/medgen/856702" ref="tree=MeSH" title="MedGen record for Non-familial Idiopathic Tall Stature">Non-familial Idiopathic Tall Stature</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/376550" ref="tree=MeSH" title="MedGen record for Overgrowth">Overgrowth</a></span></li><li><span class="TLline"><a href="/medgen/868957" ref="tree=MeSH" title="MedGen record for Proportionate tall stature">Proportionate tall stature</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</div>
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<div class="portlet mgSection" id="ID_112">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_140932"><div><strong>Worth disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>140932</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.">C0432273</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal dominant endosteal hyperostosis is a generalized bone dysplasia characterized by a cortical thickening of the long bones, with no alteration in external shape, and a remarkable resistance of the bone to fracture. The skeleton is normal in childhood. Facial metamorphoses occur in adolescence, as the forehead flattens, the mandible becomes elongated, and the gonial angle decreases. An enlarging osseous prominence (torus palatinus) develops in the hard palate, which may lead to malocclusion or loss of teeth (summary by Van Wesenbeeck et al., 2003).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/140932">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_348322"><div><strong>Tarsal-carpal coalition syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>348322</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.">C1861305</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Tarsal-carpal coalition syndrome is a rare, inherited bone disorder that affects primarily the hands and feet. Several individual bones make up each wrist (carpal bones) and ankle (tarsal bones). In tarsal-carpal coalition syndrome, the carpal bones fuse together, as do the tarsal bones, which causes stiffness and immobility of the hands and feet. Symptoms of the condition can become apparent in infancy, and they worsen with age. The severity of the symptoms can vary, even among members of the same family.\n\nIn this condition, fusion at the joints between the bones that make up each finger and toe (symphalangism) can also occur. Consequently, the fingers and toes become stiff and difficult to bend. Stiffness of the pinky fingers and toes (fifth digits) is usually noticeable first. The joints at the base of the pinky fingers and toes fuse first, and slowly, the other joints along the length of these digits may also be affected. Progressively, the bones in the fourth, third, and second digits (the ring finger, middle finger, and forefinger, and the corresponding toes) become fused. The thumb and big toe are usually not involved. Affected individuals have increasing trouble forming a fist, and walking often becomes painful and difficult. Occasionally, there is also fusion of bones in the upper and lower arm at the elbow joint (humeroradial fusion). Less common features of tarsal-carpal coalition syndrome include short stature or the development of hearing loss.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/348322">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_382715"><div><strong>Chromosome 1q21.1 duplication syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>382715</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.">C2675891</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">1q21.1 microduplication is a chromosomal change in which a small amount of genetic material on chromosome 1 is abnormally copied (duplicated). The duplication occurs on the long (q) arm of the chromosome at a location designated q21.1.\n\nSome people with a 1q21.1 microduplication have developmental delay and intellectual disability that is typically mild to moderate. Individuals with this condition can also have features of autism spectrum disorder. These disorders are characterized by impaired communication and socialization skills, as well as delayed development of speech and language. Expressive language skills (vocabulary and the production of speech) tend to be more impaired than receptive language skills (the ability to understand speech) in affected individuals. In childhood, 1q21.1 microduplications may also be associated with an increased risk of attention-deficit/hyperactivity disorder (ADHD) and other behavioral problems. Psychiatric disorders such as schizophrenia or mood disorders such as anxiety or depression occur in some affected individuals, usually during adulthood. Rarely, recurrent seizures (epilepsy) occur in people with a 1q21.1 microduplication.\n\nSome individuals with a 1q21.1 microduplication are born with malformations of the heart, including a particular combination of heart defects known as tetralogy of Fallot. Less commonly, other physical malformations such as the urethra opening on the underside of the penis (hypospadias) in males, inward- and upward-turning feet (clubfeet), or misalignment of the hip joint (hip dysplasia) are present at birth. Individuals with a 1q21.1 microduplication may also have a larger than average head size or taller than average adult stature. Some have slightly unusual facial features such as wide-set eyes or low-set ears. As adults, individuals with a 1q21.1 microduplication may be prone to develop cysts, swollen and knotted (varicose) veins, or carpal tunnel syndrome, which is characterized by numbness, tingling, and weakness in the hands and fingers. However, there is no particular pattern of physical abnormalities that characterizes 1q21.1 microduplications. Signs and symptoms related to the chromosomal change vary even among affected members of the same family. Some people with the duplication have no identified physical, intellectual, or behavioral abnormalities.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/382715">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1616860"><div><strong>Microcephaly 19, primary, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1616860</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.">C4540488</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive primary microcephaly-19 (MCPH19) is a rare congenital brain defect resulting in a reduction of occipitofrontal head circumference by at least 3 standard deviations, severe developmental delay, failure to thrive, cortical blindness, and spasticity (DiStasio et al., 2017). For a general phenotypic description and a discussion of genetic heterogeneity of primary microcephaly, see MCPH1 (251200).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1616860">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_382715" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chromosome 1q21.1 duplication syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1616860" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Microcephaly 19, primary, autosomal recessive</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_348322" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Tarsal-carpal coalition syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_140932" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Worth disease</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/33382560">Eating Disorders in Primary Care: Diagnosis and Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Klein DA,
|
||
Sylvester JE,
|
||
Schvey NA</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2021 Jan 1;103(1):22-32.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33382560" target="_blank">33382560</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31169958">ISUOG Practice Guidelines: ultrasound assessment of fetal biometry and growth.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Salomon LJ,
|
||
Alfirevic Z,
|
||
Da Silva Costa F,
|
||
Deter RL,
|
||
Figueras F,
|
||
Ghi T,
|
||
Glanc P,
|
||
Khalil A,
|
||
Lee W,
|
||
Napolitano R,
|
||
Papageorghiou A,
|
||
Sotiriadis A,
|
||
Stirnemann J,
|
||
Toi A,
|
||
Yeo G</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
|
||
2019 Jun;53(6):715-723.
|
||
doi: 10.1002/uog.20272.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31169958" target="_blank">31169958</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27585961">Diagnosis and management of Silver-Russell syndrome: first international consensus statement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wakeling EL,
|
||
Brioude F,
|
||
Lokulo-Sodipe O,
|
||
O'Connell SM,
|
||
Salem J,
|
||
Bliek J,
|
||
Canton AP,
|
||
Chrzanowska KH,
|
||
Davies JH,
|
||
Dias RP,
|
||
Dubern B,
|
||
Elbracht M,
|
||
Giabicani E,
|
||
Grimberg A,
|
||
Grønskov K,
|
||
Hokken-Koelega AC,
|
||
Jorge AA,
|
||
Kagami M,
|
||
Linglart A,
|
||
Maghnie M,
|
||
Mohnike K,
|
||
Monk D,
|
||
Moore GE,
|
||
Murray PG,
|
||
Ogata T,
|
||
Petit IO,
|
||
Russo S,
|
||
Said E,
|
||
Toumba M,
|
||
Tümer Z,
|
||
Binder G,
|
||
Eggermann T,
|
||
Harbison MD,
|
||
Temple IK,
|
||
Mackay DJ,
|
||
Netchine I</span><br />
|
||
<span class="medgenPMjournal">Nat Rev Endocrinol</span>
|
||
2017 Feb;13(2):105-124.
|
||
Epub 2016 Sep 2
|
||
doi: 10.1038/nrendo.2016.138.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27585961" target="_blank">27585961</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormality%20of%20body%20height)%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 (356)</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/33714405">The height as an independent risk factor of atrial fibrillation: A review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sohail H,
|
||
Hassan SM,
|
||
Yaqoob U,
|
||
Hassan Z</span><br />
|
||
<span class="medgenPMjournal">Indian Heart J</span>
|
||
2021 Jan-Feb;73(1):22-25.
|
||
Epub 2020 Nov 12
|
||
doi: 10.1016/j.ihj.2020.11.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33714405" target="_blank">33714405</a><a href="/pmc/articles/PMC7961249" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31230692">Tall Stature in Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leung AKC,
|
||
Leung AAC,
|
||
Hon KL</span><br />
|
||
<span class="medgenPMjournal">Adv Pediatr</span>
|
||
2019 Aug;66:161-176.
|
||
Epub 2019 May 17
|
||
doi: 10.1016/j.yapd.2019.04.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31230692" target="_blank">31230692</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29126609">Meta-analysis of adult height and birth length in schizophrenia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Latham K,
|
||
Kirkpatrick B</span><br />
|
||
<span class="medgenPMjournal">Schizophr Res</span>
|
||
2018 May;195:110-114.
|
||
Epub 2017 Nov 7
|
||
doi: 10.1016/j.schres.2017.09.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29126609" target="_blank">29126609</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20371592">Overgrowth.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Verge CF,
|
||
Mowat D</span><br />
|
||
<span class="medgenPMjournal">Arch Dis Child</span>
|
||
2010 Jun;95(6):458-63.
|
||
Epub 2010 Apr 6
|
||
doi: 10.1136/adc.2009.157693.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20371592" target="_blank">20371592</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4581634">Smoking, pregnancy, and development of the offspring.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Nutr Rev</span>
|
||
1973 May;31(5):143-5.
|
||
doi: 10.1111/j.1753-4887.1973.tb05155.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4581634" target="_blank">4581634</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20body%20height%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 (3581)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32748612">Tall stature in children and adolescents.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Urakami T</span><br />
|
||
<span class="medgenPMjournal">Minerva Pediatr</span>
|
||
2020 Dec;72(6):472-483.
|
||
Epub 2020 Aug 4
|
||
doi: 10.23736/S0026-4946.20.05971-X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32748612" target="_blank">32748612</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31230692">Tall Stature in Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leung AKC,
|
||
Leung AAC,
|
||
Hon KL</span><br />
|
||
<span class="medgenPMjournal">Adv Pediatr</span>
|
||
2019 Aug;66:161-176.
|
||
Epub 2019 May 17
|
||
doi: 10.1016/j.yapd.2019.04.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31230692" target="_blank">31230692</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26621648">Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 7: Aortic Diseases, Including Marfan Syndrome: A Scientific Statement From the American Heart Association and American College of Cardiology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Braverman AC,
|
||
Harris KM,
|
||
Kovacs RJ,
|
||
Maron BJ;
|
||
American Heart Association Electrocardiography and Arrhythmias Committee of Council on Clinical Cardiology, Council on Cardiovascular Disease in Young, Council on Cardiovascular and Stroke Nursing, Council on Functional Genomics and Translational Biology, and American College of Cardiology</span><br />
|
||
<span class="medgenPMjournal">Circulation</span>
|
||
2015 Dec 1;132(22):e303-9.
|
||
Epub 2015 Nov 2
|
||
doi: 10.1161/CIR.0000000000000243.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26621648" target="_blank">26621648</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18593751">Turner syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Loscalzo ML</span><br />
|
||
<span class="medgenPMjournal">Pediatr Rev</span>
|
||
2008 Jul;29(7):219-27.
|
||
doi: 10.1542/pir.29-7-219.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18593751" target="_blank">18593751</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10826617">The KBG syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Smithson SF,
|
||
Thompson EM,
|
||
McKinnon AG,
|
||
Smith IS,
|
||
Winter RM</span><br />
|
||
<span class="medgenPMjournal">Clin Dysmorphol</span>
|
||
2000 Apr;9(2):87-91.
|
||
doi: 10.1097/00019605-200009020-00002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10826617" target="_blank">10826617</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20body%20height%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 (2165)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/22946284">Growth hormone therapy in Turner syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Davenport ML</span><br />
|
||
<span class="medgenPMjournal">Pediatr Endocrinol Rev</span>
|
||
2012 May;9 Suppl 2:723-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22946284" target="_blank">22946284</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20010965">Growth and development: congenital adrenal hyperplasia-glucocorticoids and height.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Speiser PW</span><br />
|
||
<span class="medgenPMjournal">Nat Rev Endocrinol</span>
|
||
2010 Jan;6(1):14-5.
|
||
doi: 10.1038/nrendo.2009.242.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20010965" target="_blank">20010965</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15758537">Growth hormone therapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bajpai A,
|
||
Menon PS</span><br />
|
||
<span class="medgenPMjournal">Indian J Pediatr</span>
|
||
2005 Feb;72(2):139-44.
|
||
doi: 10.1007/BF02760699.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15758537" target="_blank">15758537</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12807497">Growth hormone therapy for syndromic disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kelnar CJ</span><br />
|
||
<span class="medgenPMjournal">Clin Endocrinol (Oxf)</span>
|
||
2003 Jul;59(1):12-21.
|
||
doi: 10.1046/j.1365-2265.2003.01756.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12807497" target="_blank">12807497</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4284784">Studies of anabolic steroids. 3. The effect of oxandrolone on height and skeletal maturation in mongoloid children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ray CG,
|
||
Kirschvink JF,
|
||
Waxman SH,
|
||
Kelley VC</span><br />
|
||
<span class="medgenPMjournal">Am J Dis Child</span>
|
||
1965 Dec;110(6):618-23.
|
||
doi: 10.1001/archpedi.1965.02090030646005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4284784" target="_blank">4284784</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20body%20height%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 (1623)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32748612">Tall stature in children and adolescents.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Urakami T</span><br />
|
||
<span class="medgenPMjournal">Minerva Pediatr</span>
|
||
2020 Dec;72(6):472-483.
|
||
Epub 2020 Aug 4
|
||
doi: 10.23736/S0026-4946.20.05971-X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32748612" target="_blank">32748612</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27855999">Assessment of Growth 6 Years after the Norwood Procedure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Burch PT,
|
||
Ravishankar C,
|
||
Newburger JW,
|
||
Lambert LM,
|
||
Pemberton VL,
|
||
Granger S,
|
||
Floh AA,
|
||
Anderson JB,
|
||
Hill GD,
|
||
Hill KD,
|
||
Oster ME,
|
||
Lewis AB,
|
||
Schumacher KR,
|
||
Zyblewski SC,
|
||
Davies RR,
|
||
Jacobs JP,
|
||
Lai WW,
|
||
Minich LL;
|
||
Pediatric Heart Network Investigators</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2017 Jan;180:270-274.e6.
|
||
Epub 2016 Nov 14
|
||
doi: 10.1016/j.jpeds.2016.09.048.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27855999" target="_blank">27855999</a><a href="/pmc/articles/PMC5183480" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2939736">Long-term follow-up of patients with gastroschisis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Swartz KR,
|
||
Harrison MW,
|
||
Campbell JR,
|
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Campbell TJ</span><br />
|
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<span class="medgenPMjournal">Am J Surg</span>
|
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1986 May;151(5):546-9.
|
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doi: 10.1016/0002-9610(86)90540-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2939736" target="_blank">2939736</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4372201">Growth and body proportions in 54 boys and men with Klinefelter's syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schibler D,
|
||
Brook CG,
|
||
Kind HP,
|
||
Zachmann M,
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Prader A</span><br />
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<span class="medgenPMjournal">Helv Paediatr Acta</span>
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1974 Oct;29(4):325-33.
|
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<span class="bold">PMID: </span><a href="/pubmed/4372201" target="_blank">4372201</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/4581634">Smoking, pregnancy, and development of the offspring.</a></div>
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<div class="portlet_content ln"><span class="medgenPMjournal">Nutr Rev</span>
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1973 May;31(5):143-5.
|
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doi: 10.1111/j.1753-4887.1973.tb05155.x.
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<span class="bold">PMID: </span><a href="/pubmed/4581634" target="_blank">4581634</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20body%20height%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 (1615)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32748612">Tall stature in children and adolescents.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Urakami T</span><br />
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<span class="medgenPMjournal">Minerva Pediatr</span>
|
||
2020 Dec;72(6):472-483.
|
||
Epub 2020 Aug 4
|
||
doi: 10.23736/S0026-4946.20.05971-X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32748612" target="_blank">32748612</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27855999">Assessment of Growth 6 Years after the Norwood Procedure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Burch PT,
|
||
Ravishankar C,
|
||
Newburger JW,
|
||
Lambert LM,
|
||
Pemberton VL,
|
||
Granger S,
|
||
Floh AA,
|
||
Anderson JB,
|
||
Hill GD,
|
||
Hill KD,
|
||
Oster ME,
|
||
Lewis AB,
|
||
Schumacher KR,
|
||
Zyblewski SC,
|
||
Davies RR,
|
||
Jacobs JP,
|
||
Lai WW,
|
||
Minich LL;
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Pediatric Heart Network Investigators</span><br />
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<span class="medgenPMjournal">J Pediatr</span>
|
||
2017 Jan;180:270-274.e6.
|
||
Epub 2016 Nov 14
|
||
doi: 10.1016/j.jpeds.2016.09.048.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27855999" target="_blank">27855999</a><a href="/pmc/articles/PMC5183480" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25367382">Role of ultrasound in the management of diabetes in pregnancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ahmed B,
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||
Abushama M,
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||
Khraisheh M,
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Dudenhausen J</span><br />
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<span class="medgenPMjournal">J Matern Fetal Neonatal Med</span>
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2015;28(15):1856-63.
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Epub 2014 Nov 4
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doi: 10.3109/14767058.2014.971745.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25367382" target="_blank">25367382</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4371581">Observations from longitudinal data on growth in stature and sitting height of children with Down's syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rarick GL,
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Seefeldt V</span><br />
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<span class="medgenPMjournal">J Ment Defic Res</span>
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||
1974 Mar;18(0):63-78.
|
||
doi: 10.1111/j.1365-2788.1974.tb01219.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4371581" target="_blank">4371581</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4290694">Cerebral gigantism: endocrinological and clinical observations of six patients including a congenital giant, concordant monozygotic twins, and a child who acheived adult gigantic size.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hook EB,
|
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Reynolds JW</span><br />
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<span class="medgenPMjournal">J Pediatr</span>
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1967 Jun;70(6):900-14.
|
||
doi: 10.1016/s0022-3476(67)80263-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4290694" target="_blank">4290694</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20body%20height%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 (2514)</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">
|
||
<div class="nl"><a target="_blank" href="/pubmed/38054666">Long-term health consequences of central precocious/early puberty (CPP) and treatment with Gn-RH analogue: a short update.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Soliman AT,
|
||
Alaaraj N,
|
||
De Sanctis V,
|
||
Hamed N,
|
||
Alyafei F,
|
||
Ahmed S</span><br />
|
||
<span class="medgenPMjournal">Acta Biomed</span>
|
||
2023 Dec 5;94(6):e2023222.
|
||
doi: 10.23750/abm.v94i6.15316.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38054666" target="_blank">38054666</a><a href="/pmc/articles/PMC10734238" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37152958">GH treatment in pediatric Down syndrome: a systematic review and mini meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shaki D,
|
||
Hershkovitz E,
|
||
Tamam S,
|
||
Bollotin A,
|
||
David O,
|
||
Yalovitsky G,
|
||
Loewenthal N,
|
||
Carmon L,
|
||
Walker D,
|
||
Nowak R,
|
||
Haim A</span><br />
|
||
<span class="medgenPMjournal">Front Endocrinol (Lausanne)</span>
|
||
2023;14:1135768.
|
||
Epub 2023 Apr 21
|
||
doi: 10.3389/fendo.2023.1135768.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37152958" target="_blank">37152958</a><a href="/pmc/articles/PMC10162572" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29427215">Systematic review of quality of life in Turner syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Reis CT,
|
||
de Assumpção MS,
|
||
Guerra-Junior G,
|
||
de Lemos-Marini SHV</span><br />
|
||
<span class="medgenPMjournal">Qual Life Res</span>
|
||
2018 Aug;27(8):1985-2006.
|
||
Epub 2018 Feb 9
|
||
doi: 10.1007/s11136-018-1810-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29427215" target="_blank">29427215</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29126609">Meta-analysis of adult height and birth length in schizophrenia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Latham K,
|
||
Kirkpatrick B</span><br />
|
||
<span class="medgenPMjournal">Schizophr Res</span>
|
||
2018 May;195:110-114.
|
||
Epub 2017 Nov 7
|
||
doi: 10.1016/j.schres.2017.09.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29126609" target="_blank">29126609</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27149418">Corticosteroids for the treatment of Duchenne muscular dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matthews E,
|
||
Brassington R,
|
||
Kuntzer T,
|
||
Jichi F,
|
||
Manzur AY</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2016 May 5;2016(5):CD003725.
|
||
doi: 10.1002/14651858.CD003725.pub4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27149418" target="_blank">27149418</a><a href="/pmc/articles/PMC8580515" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20body%20height%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 (33)</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%20body%20height)%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%20body%20height%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 class="text-white" href="https://www.hhs.gov/">HHS</a>
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||
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||
<li>
|
||
<a class="text-white" href="https://www.usa.gov/">USA.gov</a>
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||
</li>
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