RT Book, Section
A1 Weiss, Shelly
A1 Hulick, Peter
A2 Murray, Michael F.
A2 Babyatsky, Mark W.
A2 Giovanni, Monica A.
A2 Alkuraya, Fowzan S.
A2 Stewart, Douglas R.
SR Print(0)
ID 1102699382
T1 Long QT Syndrome
T2 Clinical Genomics: Practical Applications in Adult Patient Care
YR 2014
FD 2014
PB McGraw-Hill Education
PP New York, NY
SN 9780071622448
LK accessbiomedicalscience.mhmedical.com/content.aspx?aid=1102699382
RD 2024/04/19
AB Disease  summary:Inherited  channelopathy  characterized  by  elongated  QT  intervals  on  electrocardiogram  (ECG),  caused  by  delayed  ventricular  repolarization  in  the  myocyte.Increased  propensity  to  syncope,  polymorphous  ventricular  tachycardia  (torsade  de  pointes),  T-wave  abnormalities,  and  sudden  death.  Unexplained  seizures  can  also  be  an  atypical  presentation.