Article
A case of term mors in utero in a chromosome 11p linked long QT syndrome family.
Genetic counseling (Geneva, Switzerland) - 1 Jan 1994
Desmyttere S, Bonduelle M, De Wolf D, Liebaers I, Lissens W
Abstract excerpt
Isolated congenital long QT syndrome is an autosomal dominant disorder characterized by recurrent syncopes, ventricular arrhythmias, or sudden death often accompanied by a prolonged QTc interval on ECG. On the occasion of a pregnancy complicated by an intra-uterine death of a full term baby with prolonged bradycardia a long QT syndrome was diagnosed in the mother. Familial examination revealed a prolonged QTc in...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
