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<meta name="keywords" content="C0020635, adenohypophyseal hyposecretion, anterior pituitary hyposecretion syndrome, deficient secretion of one or more pituitary hormones, disease or syndrome, hypopituitarism, hyposecretion syndrome, anterior pituitary, hyposecretion, adenohypophyseal, insufficiency, pituitary, pituitary deficiency, pituitary failure, pituitary hormone deficiency, pituitary hypofunction, pituitary insufficiency, 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="A condition of diminution or cessation of secretion of one or more hormones from the anterior pituitary gland. This may result from surgical or radiation ablation, non-secretory pituitary neoplasms, metastatic tumors, infarction, pituitary apoplexy, infiltrative or granulomatous processes, and other conditions." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=9386
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ConceptID=C0020635
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Hypopituitarism</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>9386</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:">C0020635</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Adenohypophyseal Hyposecretion; Anterior Pituitary Hyposecretion Syndrome; Hyposecretion Syndrome, Anterior Pituitary; Hyposecretion, Adenohypophyseal; Insufficiency, Pituitary; Pituitary Insufficiency</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Hypopituitarism (74728003); Deficient secretion of one OR more pituitary hormones (74728003); Pituitary insufficiency (74728003); Pituitary hypofunction (74728003); Pituitary deficiency (74728003); Pituitary failure (74728003)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0040075">HP:0040075</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0005152" target="_blank">MONDO:0005152</a></td></tr>
|
||
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_100">
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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">A condition of diminution or cessation of secretion of one or more hormones from the anterior pituitary gland. This may result from surgical or radiation ablation, non-secretory pituitary neoplasms, metastatic tumors, infarction, pituitary apoplexy, infiltrative or granulomatous processes, and other conditions. [from <a title="NCI Thesaurus" href="http://ncit.nci.nih.gov" class="defSource" target="_blank">NCI</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>
|
||
<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">Hypopituitarism</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/868416" ref="tree=MeSH" title="MedGen record for Abnormal nervous system morphology">Abnormal nervous system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892343" ref="tree=MeSH" title="MedGen record for Morphological central nervous system abnormality">Morphological central nervous system abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/866738" ref="tree=MeSH" title="MedGen record for Abnormal brain morphology">Abnormal brain morphology</a></span><ul><li><span class="TLline"><a href="/medgen/1843446" ref="tree=MeSH" title="MedGen record for Abnormal pituitary gland morphology">Abnormal pituitary gland morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892315" ref="tree=MeSH" title="MedGen record for Abnormality of the anterior pituitary">Abnormality of the anterior pituitary</a></span><ul><li><span class="matched_ds">Hypopituitarism</span><ul><li><span class="TLline"><a href="/medgen/871333" ref="tree=MeSH" title="MedGen record for Anterior hypopituitarism">Anterior hypopituitarism</a></span><ul><li><span class="TLline"><a href="/medgen/868057" ref="tree=MeSH" title="MedGen record for Abnormal prolactin level">Abnormal prolactin level</a></span><ul><li><span class="TLline"><a href="/medgen/75758" ref="tree=MeSH" title="MedGen record for Isolated prolactin deficiency">Isolated prolactin deficiency</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/137968" ref="tree=MeSH" title="MedGen record for Congenital isolated adrenocorticotropic hormone deficiency">Congenital isolated adrenocorticotropic hormone deficiency</a></span><ul><li><span class="TLline"><a href="/medgen/887379" ref="tree=MeSH" title="MedGen record for Acquired Adrenocorticotropic Hormone Deficiency">Acquired Adrenocorticotropic Hormone Deficiency</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1632671" ref="tree=MeSH" title="MedGen record for Gonadotropin deficiency">Gonadotropin deficiency</a></span><ul><li><span class="TLline"><a href="/medgen/394313" ref="tree=MeSH" title="MedGen record for ANE syndrome">ANE syndrome</a></span></li><li><span class="TLline"><a href="/medgen/347798" ref="tree=MeSH" title="MedGen record for Ataxia-hypogonadism-choroidal dystrophy syndrome">Ataxia-hypogonadism-choroidal dystrophy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/156019" ref="tree=MeSH" title="MedGen record for Bardet-Biedl syndrome">Bardet-Biedl syndrome</a></span></li><li><span class="TLline"><a href="/medgen/444052" ref="tree=MeSH" title="MedGen record for Brachytelephalangy-dysmorphism-Kallmann syndrome">Brachytelephalangy-dysmorphism-Kallmann syndrome</a></span></li><li><span class="TLline"><a href="/medgen/349137" ref="tree=MeSH" title="MedGen record for Cerebellar ataxia-hypogonadism syndrome">Cerebellar ataxia-hypogonadism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75567" ref="tree=MeSH" title="MedGen record for CHARGE syndrome">CHARGE syndrome</a></span></li><li><span class="TLline"><a href="/medgen/928748" ref="tree=MeSH" title="MedGen record for Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome">Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/419479" ref="tree=MeSH" title="MedGen record for Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome">Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1663043" ref="tree=MeSH" title="MedGen record for Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome">Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/957899" ref="tree=MeSH" title="MedGen record for Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome">Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/928566" ref="tree=MeSH" title="MedGen record for Kallmann syndrome-heart disease syndrome">Kallmann syndrome-heart disease syndrome</a></span></li><li><span class="TLline"><a href="/medgen/44078" ref="tree=MeSH" title="MedGen record for Laurence-Moon syndrome">Laurence-Moon syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1778114" ref="tree=MeSH" title="MedGen record for Martsolf syndrome 1">Martsolf syndrome 1</a></span></li><li><span class="TLline"><a href="/medgen/419697" ref="tree=MeSH" title="MedGen record for Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome">Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/863698" ref="tree=MeSH" title="MedGen record for Polyendocrine-polyneuropathy syndrome">Polyendocrine-polyneuropathy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/46057" ref="tree=MeSH" title="MedGen record for Prader-Willi syndrome">Prader-Willi syndrome</a></span></li><li><span class="TLline"><a href="/medgen/83337" ref="tree=MeSH" title="MedGen record for Woodhouse-Sakati syndrome">Woodhouse-Sakati syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/69171" ref="tree=MeSH" title="MedGen record for Panhypopituitarism">Panhypopituitarism</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/8506" ref="tree=MeSH" title="MedGen record for Pituitary dwarfism">Pituitary dwarfism</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_350933"><div><strong>Acromelic frontonasal dysostosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>350933</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.">C1863616</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Verloes et al. (1992) described a rare variant of frontonasal dysplasia (see FND1, 136760), designated acromelic frontonasal dysplasia (AFND), in which similar craniofacial anomalies are associated with variable central nervous system malformations and limb defects including tibial hypoplasia/aplasia, talipes equinovarus, and preaxial polydactyly of the feet.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/350933">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_414421"><div><strong>Pituitary hormone deficiency, combined, 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>414421</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.">C2751608</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Combined pituitary hormone deficiency (CPHD) in man denotes impaired production of growth hormone (GH; 139250) and one or more of the other 5 anterior pituitary hormones. Mutations of the POU1F1 gene in the human and Pit1 in the mouse are responsible for pleiotropic deficiencies of GH, prolactin (PRL; 176760), and thyroid-stimulating hormone (TSH; see 188540), while the production of adrenocorticotrophic hormone (ACTH; see 176830), luteinizing hormone (LH; 152780), and follicle-stimulating hormone (FSH; 136530) are preserved (Wu et al., 1998). Some patients exhibit only GH deficiency, although approximately 50% of isolated GH deficiency progresses to CPHD (Gergics et al., 2021). In infancy severe growth deficiency from birth as well as distinctive facial features with prominent forehead, marked midfacial hypoplasia with depressed nasal bridge, deep-set eyes, and a short nose with anteverted nostrils and hypoplastic pituitary gland by MRI examination can be seen (Aarskog et al., 1997). Some cases present with severe mental retardation along with short stature (Radovick et al., 1992). Reviews Voss and Rosenfeld (1992) reviewed the development and differentiation of the 5 pituitary cell types: galactotropes, gonadotropes, corticotropes, thyrotropes, and somatotropes. As indicated by the mutations in PIT1 described later, combined pituitary hormone deficiency can have either autosomal dominant or autosomal recessive inheritance, depending on the part of the PIT1 molecule affected by the mutation. Some mutations have a dominant-negative effect. Genetic Heterogeneity of Combined Pituitary Hormone Deficiency CPHD2 (262600), associated with hypogonadism, is caused by mutation in the PROP1 gene (601538). CPHD3 (221750), which is associated with rigid cervical spine and variable sensorineural deafness, is caused by mutation in the LHX3 gene (600577). CPHD4 (262700) is caused by mutation in the LHX4 gene (602146). CPHD5 (see septooptic dysplasia, 182230) is caused by mutation in the HESX1 gene (601802). CPHD6 (613986) is caused by mutation in the OTX2 gene (600037). CPHD7 (618160) is caused by mutation in the RNPC3 gene (618016). CPHD8 (620303) is caused by mutation in the ROBO1 gene (602430).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/414421">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_856021"><div><strong>X-linked acrogigantism due to Xq26 microduplication</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>856021</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.">C3891556</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">X-linked acrogigantism is the occurrence of pituitary gigantism in an individual heterozygous or hemizygous for a germline or somatic duplication of GPR101. X-linked acrogigantism is characterized by acceleration of linear growth in early childhood – in most cases during the first two years of life – due to growth hormone (GH) excess. Most individuals with X-linked acrogigantism present with associated hyperprolactinemia due to a mixed GH- and prolactin-secreting pituitary adenoma with or without associated hyperplasia; less commonly they develop diffuse hyperplasia of the GH- and prolactin-secreting pituitary cells without a pituitary adenoma. Most affected individuals are females. Growth acceleration is the main presenting feature; other frequently observed clinical features include enlargement of hands and feet, coarsening of the facial features, and increased appetite. Neurologic signs or symptoms are rarely present. Untreated X-linked acrogigantism can lead to markedly increased stature, with obvious severe physical and psychological sequelae.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/856021">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_862916"><div><strong>Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>862916</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.">C4014479</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome is a rare, genetic developmental defect during embryogenesis disorder characterized primarily by congenital hypopituitarism and/or postaxial polydactyly. It can be associated with short stature, delayed bone age, hypogonadotropic hypogonadism, and/or midline facial defects (e.g. hypotelorism, mild midface hypoplasia, flat nasal bridge, and cleft lip and/or palate). Hypoplastic anterior pituitary and ectopic posterior pituitary lobe are frequent findings on MRI examination.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/862916">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1634824"><div><strong>Myopathy, lactic acidosis, and sideroblastic anemia 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1634824</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.">C4551958</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Myopathy, lactic acidosis, and sideroblastic anemia (MLASA) is a rare autosomal recessive oxidative phosphorylation disorder specific to skeletal muscle and bone marrow (Bykhovskaya et al., 2004). Genetic Heterogeneity of Myopathy, Lactic Acidosis, and Sideroblastic Anemia MLASA2 (613561) is caused by mutation in the YARS2 gene (610957) on chromosome 12p11. MLASA3 (500011) is caused by heteroplasmic mutation in the mitochondrially-encoded MTATP6 gene (516060).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1634824">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1770895"><div><strong>Rajab interstitial lung disease with brain calcifications 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1770895</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.">C5436603</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Rajab interstitial lung disease with brain calcifications-2 (RILDBC2) is an autosomal recessive disorder characterized by growth delay, interstitial lung disease, liver disease, and abnormal brain MRI findings, including brain calcifications and periventricular cysts (Krenke et al., 2019). For a discussion of genetic heterogeneity of RILDBC, see RILDBC1 (613658).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1770895">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1787149"><div><strong>Hypertriglyceridemia 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1787149</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.">C5444012</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1787149">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1845412"><div><strong>Diabetes, deafness, developmental delay, and short stature syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1845412</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.">C5882732</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Diabetes, deafness, developmental delay, and short stature syndrome (DDDS) is characterized by childhood-onset autoantibody-negative diabetes mellitus and bilateral sensorineural deafness, as well as short stature, microcephaly, and developmental delay (Montaser et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1845412">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_350933" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acromelic frontonasal dysostosis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1845412" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Diabetes, deafness, developmental delay, and short stature syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1787149" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypertriglyceridemia 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1634824" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Myopathy, lactic acidosis, and sideroblastic anemia 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_414421" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pituitary hormone deficiency, combined, 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_862916" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1770895" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Rajab interstitial lung disease with brain calcifications 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_856021" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">X-linked acrogigantism due to Xq26 microduplication</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/37341019">Pediatric Moderate and Severe Traumatic Brain Injury: A Systematic Review of Clinical Practice Guideline Recommendations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ben Abdeljelil A,
|
||
Freire GC,
|
||
Yanchar N,
|
||
Turgeon AF,
|
||
Beno S,
|
||
Bérubé M,
|
||
Stang A,
|
||
Stelfox T,
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||
Zemek R,
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||
Beaulieu E,
|
||
Gagnon IJ,
|
||
Gabbe B,
|
||
Lauzier F,
|
||
Labrosse M,
|
||
Tardif PA,
|
||
Deshommes T,
|
||
Gnanvi J,
|
||
Moore L</span><br />
|
||
<span class="medgenPMjournal">J Neurotrauma</span>
|
||
2023 Nov;40(21-22):2270-2281.
|
||
Epub 2023 Aug 16
|
||
doi: 10.1089/neu.2023.0149.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37341019" target="_blank">37341019</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37097352">Diagnosis and Management of Pituitary Adenomas: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tritos NA,
|
||
Miller KK</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2023 Apr 25;329(16):1386-1398.
|
||
doi: 10.1001/jama.2023.5444.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37097352" target="_blank">37097352</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28170483">Diagnosis and Treatment of Pituitary Adenomas: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Molitch ME</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2017 Feb 7;317(5):516-524.
|
||
doi: 10.1001/jama.2016.19699.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28170483" target="_blank">28170483</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22hypopituitarism%22%5Btiab%3A~0%5D)%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 (291)</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/36742387">Sheehan syndrome: Cardiovascular and metabolic comorbidities.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Laway BA,
|
||
Baba MS</span><br />
|
||
<span class="medgenPMjournal">Front Endocrinol (Lausanne)</span>
|
||
2023;14:1086731.
|
||
Epub 2023 Jan 20
|
||
doi: 10.3389/fendo.2023.1086731.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36742387" target="_blank">36742387</a><a href="/pmc/articles/PMC9895769" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31745969">Pituitary apoplexy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wichlińska-Lubińska M,
|
||
Kozera G</span><br />
|
||
<span class="medgenPMjournal">Neurol Neurochir Pol</span>
|
||
2019;53(6):413-420.
|
||
Epub 2019 Nov 20
|
||
doi: 10.5603/PJNNS.a2019.0054.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31745969" target="_blank">31745969</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27736313">Hormonal Replacement in Hypopituitarism in Adults: An Endocrine Society Clinical Practice Guideline.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fleseriu M,
|
||
Hashim IA,
|
||
Karavitaki N,
|
||
Melmed S,
|
||
Murad MH,
|
||
Salvatori R,
|
||
Samuels MH</span><br />
|
||
<span class="medgenPMjournal">J Clin Endocrinol Metab</span>
|
||
2016 Nov;101(11):3888-3921.
|
||
Epub 2016 Oct 13
|
||
doi: 10.1210/jc.2016-2118.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27736313" target="_blank">27736313</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17069265">Craniopharyngiomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alvarez M</span><br />
|
||
<span class="medgenPMjournal">J Neurosci Nurs</span>
|
||
2006 Oct;38(5):362-8.
|
||
doi: 10.1097/01376517-200610000-00007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17069265" target="_blank">17069265</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11680796">Hypopituitarism and atherosclerosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Elhadd TA,
|
||
Abdu TA,
|
||
Clayton R</span><br />
|
||
<span class="medgenPMjournal">Ann Med</span>
|
||
2001 Oct;33(7):477-85.
|
||
doi: 10.3109/07853890109002097.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11680796" target="_blank">11680796</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypopituitarism%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 (2463)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38735295">Hypopituitarism.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fleseriu M,
|
||
Christ-Crain M,
|
||
Langlois F,
|
||
Gadelha M,
|
||
Melmed S</span><br />
|
||
<span class="medgenPMjournal">Lancet</span>
|
||
2024 Jun 15;403(10444):2632-2648.
|
||
Epub 2024 May 9
|
||
doi: 10.1016/S0140-6736(24)00342-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38735295" target="_blank">38735295</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34125791">Sheehan syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Laway BA,
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<div class="nl"><a target="_blank" href="/pubmed/31082937">Diagnosis and management of hypopituitarism.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/24052242">Pituitary incidentalomas.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Vance ML</span><br />
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypopituitarism%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 (3271)</a></div><h3 class="subhead">Therapy</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37373261">Management of Neonatal Isolated and Combined Growth Hormone Deficiency: Current Status.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/31745969">Pituitary apoplexy.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Vespa P;
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<span class="bold">PMID: </span><a href="/pubmed/21800209" target="_blank">21800209</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/9672293">Pituitary insufficiency.</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypopituitarism%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 (2455)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/33423151">Neuroimmunological adverse events associated with immune checkpoint inhibitor: a retrospective, pharmacovigilance study using FAERS database.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mikami T,
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Asada M,
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Niimura T,
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Zamami Y,
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Levy M,
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<span class="bold">PMID: </span><a href="/pubmed/33423151" target="_blank">33423151</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/29344907">Silent corticotroph adenomas.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Ben-Shlomo A,
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<div class="nl"><a target="_blank" href="/pubmed/21474686">Pituitary incidentaloma: an endocrine society clinical practice guideline.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Freda PU,
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Katznelson L,
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<div class="nl"><a target="_blank" href="/pubmed/1632922">Incidental pituitary macroadenomas.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Chacko AG,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypopituitarism%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 (1425)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37097352">Diagnosis and Management of Pituitary Adenomas: A Review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Tritos NA,
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Miller KK</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/37097352" target="_blank">37097352</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/30929221">Traumatic brain injury: neuropathological, neurocognitive and neurobehavioral sequelae.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Pavlovic D,
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Pekic S,
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<span class="bold">PMID: </span><a href="/pubmed/30929221" target="_blank">30929221</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/23245206">Sheehan's syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Kilicli F,
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<div class="nl"><a target="_blank" href="/pubmed/21809154">Endocrine function following acute SAH.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Vespa P;
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Participants in the International Multi-Disciplinary Consensus Conference on the Critical Care Management of Subarachnoid Hemorrhage</span><br />
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<span class="medgenPMjournal">Neurocrit Care</span>
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2011 Sep;15(2):361-4.
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<div class="nl"><a target="_blank" href="/pubmed/21800209">SAH pituitary adrenal dysfunction.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Vespa P;
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Participants in the International Multi-Disciplinary Consensus Conference on the Critical Care Management of Subarachnoid Hemorrhage</span><br />
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doi: 10.1007/s12028-011-9595-7.
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<span class="bold">PMID: </span><a href="/pubmed/21800209" target="_blank">21800209</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypopituitarism%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 (1503)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<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/37468264">Association of nonalcoholic fatty liver disease and growth hormone deficiency: a systematic review and meta-analysis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Kong T,
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Gu Y,
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Sun L,
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Zhou R,
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Li J,
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Shi J</span><br />
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<span class="medgenPMjournal">Endocr J</span>
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2023 Oct 30;70(10):959-967.
|
||
Epub 2023 Jul 20
|
||
doi: 10.1507/endocrj.EJ23-0157.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37468264" target="_blank">37468264</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37341019">Pediatric Moderate and Severe Traumatic Brain Injury: A Systematic Review of Clinical Practice Guideline Recommendations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ben Abdeljelil A,
|
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Freire GC,
|
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Yanchar N,
|
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Turgeon AF,
|
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Beno S,
|
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Bérubé M,
|
||
Stang A,
|
||
Stelfox T,
|
||
Zemek R,
|
||
Beaulieu E,
|
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Gagnon IJ,
|
||
Gabbe B,
|
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Lauzier F,
|
||
Labrosse M,
|
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Tardif PA,
|
||
Deshommes T,
|
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Gnanvi J,
|
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Moore L</span><br />
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<span class="medgenPMjournal">J Neurotrauma</span>
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2023 Nov;40(21-22):2270-2281.
|
||
Epub 2023 Aug 16
|
||
doi: 10.1089/neu.2023.0149.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37341019" target="_blank">37341019</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36809201">Neuropathy, Ataxia, and Retinitis Pigmentosa Syndrome.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Finsterer J</span><br />
|
||
<span class="medgenPMjournal">J Clin Neuromuscul Dis</span>
|
||
2023 Mar 1;24(3):140-146.
|
||
doi: 10.1097/CND.0000000000000422.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36809201" target="_blank">36809201</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25534889">Silent corticotroph adenomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cooper O</span><br />
|
||
<span class="medgenPMjournal">Pituitary</span>
|
||
2015 Apr;18(2):225-31.
|
||
doi: 10.1007/s11102-014-0624-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25534889" target="_blank">25534889</a><a href="/pmc/articles/PMC4376561" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24052242">Pituitary incidentalomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Scangas GA,
|
||
Laws ER Jr</span><br />
|
||
<span class="medgenPMjournal">Pituitary</span>
|
||
2014 Oct;17(5):486-91.
|
||
doi: 10.1007/s11102-013-0517-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24052242" target="_blank">24052242</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypopituitarism%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 (104)</a></div></div>
|
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</div>
|
||
</div></div></div></div></div></div></div>
|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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