Severe aortic regurgitation and partial anomalous pulmonary venous connection in a Turner syndrome patient
Identifieur interne : 000162 ( Pmc/Corpus ); précédent : 000161; suivant : 000163Severe aortic regurgitation and partial anomalous pulmonary venous connection in a Turner syndrome patient
Auteurs : Kanhua Yin ; Jun Li ; Kai Zhu ; Yulin Wang ; Hao Lai ; Chunsheng WangSource :
- Journal of Thoracic Disease [ 2072-1439 ] ; 2015.
Abstract
Turner syndrome (TS) is one of the most common sex chromosome diseases. Short stature (if untreated) and ovarian dysgenesis (streak ovary) are two typical clinical manifestations of these patients. A variety of cardiovascular abnormalities has been found associated with TS. We report a 29-year-old TS patient with severe aortic regurgitation, bicuspid aortic valve (BAV) and partial anomalous pulmonary venous connection (PAPVC). We discuss the diagnostic and surgical management of cardiovascular complications in TS patients.
Url:
DOI: 10.3978/j.issn.2072-1439.2015.11.04
PubMed: 26716053
PubMed Central: 4669282
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PMC:4669282Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Severe aortic regurgitation and partial anomalous pulmonary venous connection in a Turner syndrome patient</title>
<author><name sortKey="Yin, Kanhua" sort="Yin, Kanhua" uniqKey="Yin K" first="Kanhua" last="Yin">Kanhua Yin</name>
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<author><name sortKey="Li, Jun" sort="Li, Jun" uniqKey="Li J" first="Jun" last="Li">Jun Li</name>
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<author><name sortKey="Zhu, Kai" sort="Zhu, Kai" uniqKey="Zhu K" first="Kai" last="Zhu">Kai Zhu</name>
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<author><name sortKey="Wang, Yulin" sort="Wang, Yulin" uniqKey="Wang Y" first="Yulin" last="Wang">Yulin Wang</name>
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<author><name sortKey="Lai, Hao" sort="Lai, Hao" uniqKey="Lai H" first="Hao" last="Lai">Hao Lai</name>
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<author><name sortKey="Wang, Chunsheng" sort="Wang, Chunsheng" uniqKey="Wang C" first="Chunsheng" last="Wang">Chunsheng Wang</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Severe aortic regurgitation and partial anomalous pulmonary venous connection in a Turner syndrome patient</title>
<author><name sortKey="Yin, Kanhua" sort="Yin, Kanhua" uniqKey="Yin K" first="Kanhua" last="Yin">Kanhua Yin</name>
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<author><name sortKey="Li, Jun" sort="Li, Jun" uniqKey="Li J" first="Jun" last="Li">Jun Li</name>
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<author><name sortKey="Zhu, Kai" sort="Zhu, Kai" uniqKey="Zhu K" first="Kai" last="Zhu">Kai Zhu</name>
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<author><name sortKey="Wang, Yulin" sort="Wang, Yulin" uniqKey="Wang Y" first="Yulin" last="Wang">Yulin Wang</name>
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<author><name sortKey="Lai, Hao" sort="Lai, Hao" uniqKey="Lai H" first="Hao" last="Lai">Hao Lai</name>
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<author><name sortKey="Wang, Chunsheng" sort="Wang, Chunsheng" uniqKey="Wang C" first="Chunsheng" last="Wang">Chunsheng Wang</name>
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<series><title level="j">Journal of Thoracic Disease</title>
<idno type="ISSN">2072-1439</idno>
<idno type="eISSN">2077-6624</idno>
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<front><div type="abstract" xml:lang="en"><p>Turner syndrome (TS) is one of the most common sex chromosome diseases. Short stature (if untreated) and ovarian dysgenesis (streak ovary) are two typical clinical manifestations of these patients. A variety of cardiovascular abnormalities has been found associated with TS. We report a 29-year-old TS patient with severe aortic regurgitation, bicuspid aortic valve (BAV) and partial anomalous pulmonary venous connection (PAPVC). We discuss the diagnostic and surgical management of cardiovascular complications in TS patients.</p>
</div>
</front>
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<pmc article-type="case-report"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Thorac Dis</journal-id>
<journal-id journal-id-type="iso-abbrev">J Thorac Dis</journal-id>
<journal-id journal-id-type="publisher-id">JTD</journal-id>
<journal-title-group><journal-title>Journal of Thoracic Disease</journal-title>
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<issn pub-type="ppub">2072-1439</issn>
<issn pub-type="epub">2077-6624</issn>
<publisher><publisher-name>AME Publishing Company</publisher-name>
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<article-id pub-id-type="pmc">4669282</article-id>
<article-id pub-id-type="publisher-id">jtd-07-11-E548</article-id>
<article-id pub-id-type="doi">10.3978/j.issn.2072-1439.2015.11.04</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group><article-title>Severe aortic regurgitation and partial anomalous pulmonary venous connection in a Turner syndrome patient</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Yin</surname>
<given-names>Kanhua</given-names>
</name>
<xref ref-type="author-notes" rid="afn1">*</xref>
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<contrib contrib-type="author"><name><surname>Li</surname>
<given-names>Jun</given-names>
</name>
<xref ref-type="author-notes" rid="afn1">*</xref>
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<contrib contrib-type="author"><name><surname>Zhu</surname>
<given-names>Kai</given-names>
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<contrib contrib-type="author"><name><surname>Wang</surname>
<given-names>Yulin</given-names>
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<contrib contrib-type="author" corresp="yes"><name><surname>Lai</surname>
<given-names>Hao</given-names>
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<contrib contrib-type="author" corresp="yes"><name><surname>Wang</surname>
<given-names>Chunsheng</given-names>
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<aff id="aff1">Department of Cardiac Surgery, Shanghai Institute of Cardiovascular Disease, Zhongshan Hospital, Fudan University, Shanghai 200032,<country>China</country>
</aff>
</contrib-group>
<author-notes><fn id="afn1"><label>*</label>
<p>These authors contributed equally to this work.</p>
</fn>
<corresp id="cor1"><italic>Correspondence to:</italic>
Hao Lai, MD, PhD; Chunsheng Wang, MD. Department of Cardiac Surgery, Shanghai Institute of Cardiovascular Disease, Zhongshan Hospital, Fudan University, No. 180 Fenglin Road, Shanghai 200032, China. Email: <email xlink:href="lai.hao@zs-hospital.sh.cn">lai.hao@zs-hospital.sh.cn</email>
; <email xlink:href="cswang@medmail.com.cn">cswang@medmail.com.cn</email>
.</corresp>
</author-notes>
<pub-date pub-type="epub-ppub"><month>11</month>
<year>2015</year>
</pub-date>
<pmc-comment>Fake ppub date generated by PMC from publisher
pub-date/@pub-type='epub-ppub' </pmc-comment>
<pub-date pub-type="ppub"><month>11</month>
<year>2015</year>
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<volume>7</volume>
<issue>11</issue>
<fpage>E548</fpage>
<lpage>E551</lpage>
<history><date date-type="received"><day>09</day>
<month>7</month>
<year>2015</year>
</date>
<date date-type="accepted"><day>13</day>
<month>10</month>
<year>2015</year>
</date>
</history>
<permissions><copyright-statement>2015 Journal of Thoracic Disease. All rights reserved.</copyright-statement>
<copyright-year>2015</copyright-year>
<copyright-holder>Journal of Thoracic Disease.</copyright-holder>
</permissions>
<abstract><p>Turner syndrome (TS) is one of the most common sex chromosome diseases. Short stature (if untreated) and ovarian dysgenesis (streak ovary) are two typical clinical manifestations of these patients. A variety of cardiovascular abnormalities has been found associated with TS. We report a 29-year-old TS patient with severe aortic regurgitation, bicuspid aortic valve (BAV) and partial anomalous pulmonary venous connection (PAPVC). We discuss the diagnostic and surgical management of cardiovascular complications in TS patients.</p>
</abstract>
<kwd-group kwd-group-type="author"><title>Keywords: </title>
<kwd>Turner syndrome (TS)</kwd>
<kwd>aortic regurgitation</kwd>
<kwd>bicuspid aortic valve (BAV)</kwd>
<kwd>partial anomalous pulmonary venous connection (PAPVC)</kwd>
</kwd-group>
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