Document Detail


A variant of long QT syndrome manifested as fetal tachycardia and associated with ventricular septal defect.
MedLine Citation:
PMID:  10455095     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Two patients with a novel variant of long QT syndrome are described. The clinical course was characterised by an in utero onset of ventricular tachycardia and atrioventricular block (at 26 and 30 weeks' gestational age, respectively), and an association with a ventricular septal defect. Studies of both patients' families identified relatives with prolonged QT interval, syncope, or sudden death. One patient died of intractable ventricular tachycardia at 4 days old. The other received beta blocker treatment and a pacemaker. She died suddenly at the age of 10 months. The unique association with ventricular septal defect and the malignant clinical course warrants further molecular diagnosis of this novel variant of long QT syndrome.
Authors:
M H Wu; F C Hsieh; J K Wang; M L Kau
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Heart (British Cardiac Society)     Volume:  82     ISSN:  1468-201X     ISO Abbreviation:  Heart     Publication Date:  1999 Sep 
Date Detail:
Created Date:  1999-10-07     Completed Date:  1999-10-07     Revised Date:  2008-11-20    
Medline Journal Info:
Nlm Unique ID:  9602087     Medline TA:  Heart     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  386-8     Citation Subset:  AIM; IM    
Affiliation:
Department of Pediatrics, National Taiwan University Hospital, No 7, Chung-Shen South Road, Taipei, Taiwan 100. mhwu@ha.mc.ntu.edu.tw
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MeSH Terms
Descriptor/Qualifier:
Female
Fetal Diseases / genetics*
Heart Septal Defects, Ventricular / genetics*
Humans
Infant, Newborn
Long QT Syndrome / genetics*
Pedigree
Tachycardia, Ventricular / genetics*

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