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An association with hypopituitarism and 9q subtelomere deletion syndrome
Key Clinical Message Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare o...
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Published in: | Clinical case reports 2018-12, Vol.6 (12), p.2371-2375 |
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creator | Higuchi, Shinji Takagi, Masaki Takeda, Ryojun Yoshihashi, Hiroshi Narumi, Satoshi Hasegawa, Tomonobu |
description | Key Clinical Message
Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare or relatively common presentation in patients with 9qSTDS.
Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare or relatively common presentation in patients with 9qSTDS.. |
doi_str_mv | 10.1002/ccr3.1591 |
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Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare or relatively common presentation in patients with 9qSTDS.
Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare or relatively common presentation in patients with 9qSTDS..</description><identifier>ISSN: 2050-0904</identifier><identifier>EISSN: 2050-0904</identifier><identifier>DOI: 10.1002/ccr3.1591</identifier><identifier>PMID: 30564331</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>9q subtelomere deletion syndrome ; array comparative genomic hybridization ; Case Report ; Case Reports ; central adrenal insufficiency ; hypopituitarism ; whole‐exome sequence</subject><ispartof>Clinical case reports, 2018-12, Vol.6 (12), p.2371-2375</ispartof><rights>2018 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4101-5a99fb37b1498386fd4d047f3d8381e54ba5bf12e151b1c7e6b04baa85fc043c3</citedby><cites>FETCH-LOGICAL-c4101-5a99fb37b1498386fd4d047f3d8381e54ba5bf12e151b1c7e6b04baa85fc043c3</cites><orcidid>0000-0003-1654-9463 ; 0000-0002-5062-0609</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2155574704/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2155574704?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30564331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Higuchi, Shinji</creatorcontrib><creatorcontrib>Takagi, Masaki</creatorcontrib><creatorcontrib>Takeda, Ryojun</creatorcontrib><creatorcontrib>Yoshihashi, Hiroshi</creatorcontrib><creatorcontrib>Narumi, Satoshi</creatorcontrib><creatorcontrib>Hasegawa, Tomonobu</creatorcontrib><title>An association with hypopituitarism and 9q subtelomere deletion syndrome</title><title>Clinical case reports</title><addtitle>Clin Case Rep</addtitle><description>Key Clinical Message
Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare or relatively common presentation in patients with 9qSTDS.
Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare or relatively common presentation in patients with 9qSTDS..</description><subject>9q subtelomere deletion syndrome</subject><subject>array comparative genomic hybridization</subject><subject>Case Report</subject><subject>Case Reports</subject><subject>central adrenal insufficiency</subject><subject>hypopituitarism</subject><subject>whole‐exome sequence</subject><issn>2050-0904</issn><issn>2050-0904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNp1kM9LwzAUx4Mobswd_Aek4MlDt_eapF0vwhjqhIEgeg5pmrqMrtmS1rH_3u6HYx48JXnvk897fAm5RRggQDRUytEB8hQvSDcCDiGkwC7P7h3S934BAAhJxBGuSYcCjxml2CXTcRVI760ysja2Cjamngfz7cquTN2YWjrjl4Gs8iBdB77Jal3apXY6yHWp9x_8tspdW7shV4Usve4fzx75fH76mEzD2dvL62Q8CxVDwJDLNC0ymmTI0hEdxUXOcmBJQfP2hZqzTPKswEgjxwxVouMM2poc8UIBo4r2yOPBu2qypc6VrmonS7FyZindVlhpxN9OZebiy36LOEppFEet4P4ocHbdaF-LhW1c1e4sIuScJyxpB_XIw4FSznrvdHGagCB2uYtd7mKXe8vena90In9TboHhAdiYUm__N4nJ5J3ulT82N41T</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Higuchi, Shinji</creator><creator>Takagi, Masaki</creator><creator>Takeda, Ryojun</creator><creator>Yoshihashi, Hiroshi</creator><creator>Narumi, Satoshi</creator><creator>Hasegawa, Tomonobu</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1654-9463</orcidid><orcidid>https://orcid.org/0000-0002-5062-0609</orcidid></search><sort><creationdate>201812</creationdate><title>An association with hypopituitarism and 9q subtelomere deletion syndrome</title><author>Higuchi, Shinji ; Takagi, Masaki ; Takeda, Ryojun ; Yoshihashi, Hiroshi ; Narumi, Satoshi ; Hasegawa, Tomonobu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4101-5a99fb37b1498386fd4d047f3d8381e54ba5bf12e151b1c7e6b04baa85fc043c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>9q subtelomere deletion syndrome</topic><topic>array comparative genomic hybridization</topic><topic>Case Report</topic><topic>Case Reports</topic><topic>central adrenal insufficiency</topic><topic>hypopituitarism</topic><topic>whole‐exome sequence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Higuchi, Shinji</creatorcontrib><creatorcontrib>Takagi, Masaki</creatorcontrib><creatorcontrib>Takeda, Ryojun</creatorcontrib><creatorcontrib>Yoshihashi, Hiroshi</creatorcontrib><creatorcontrib>Narumi, Satoshi</creatorcontrib><creatorcontrib>Hasegawa, Tomonobu</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Higuchi, Shinji</au><au>Takagi, Masaki</au><au>Takeda, Ryojun</au><au>Yoshihashi, Hiroshi</au><au>Narumi, Satoshi</au><au>Hasegawa, Tomonobu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An association with hypopituitarism and 9q subtelomere deletion syndrome</atitle><jtitle>Clinical case reports</jtitle><addtitle>Clin Case Rep</addtitle><date>2018-12</date><risdate>2018</risdate><volume>6</volume><issue>12</issue><spage>2371</spage><epage>2375</epage><pages>2371-2375</pages><issn>2050-0904</issn><eissn>2050-0904</eissn><abstract>Key Clinical Message
Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare or relatively common presentation in patients with 9qSTDS.
Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9qSTDS); thus, further investigations or reevaluation of clinical information, especially hormonal evaluations, are warranted to determine whether hypopituitarism is a rare or relatively common presentation in patients with 9qSTDS..</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>30564331</pmid><doi>10.1002/ccr3.1591</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-1654-9463</orcidid><orcidid>https://orcid.org/0000-0002-5062-0609</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 9q subtelomere deletion syndrome array comparative genomic hybridization Case Report Case Reports central adrenal insufficiency hypopituitarism whole‐exome sequence |
title | An association with hypopituitarism and 9q subtelomere deletion syndrome |
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