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Circulation, Vol 54, 423-430, Copyright © 1976 by American Heart Association
BJ Maron, CE Clark, RE Goldstein and SE Epstein
To investigate the possibility that a genetically transmitted cardiac
abnormality is involved in the genesis of the sudden infant death syndrome
(SIDS), 42 sets of parents who had at least one infant with SIDS were
studied by electrocardiography. Prolongation of the QT interval was present
in at least one member of 11 (26%) sets of parents. In families in which QT
interval prolongation was found in a parent, prolonged QT interval was also
present in 39% of the siblings of infants with SIDS, suggesting an
autosomal dominant pattern of inheritance. In addition, an infant with
"near-miss" SIDS showed marked prolongation of the QT interval. Thus, our
data suggest that prolonged QT interval may play a role in a considerable
proportion of sudden and unexpected infant deaths. However, definitive
confirmation of the relation between QT interval prolongation and SIDS will
require large prospective investigations.
ARTICLES
Potential role of QT interval prolongation in sudden infant death syndrome
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