Pediatr Pathol. 1994 Nov-Dec;14(6):987-95.

Sudden death in childhood due to right ventricular dysplasia: report of two cases.

Pawel BR, de Chadarévian JP, Wolk JH, Donner RM, Vogel RL, Braverman P.

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Department of Pathology, St. Christopher's Hospital for Children, Philadelphia, Pennsylvania 19134-1095.

Abstract

Two cases of sudden death due to arrhythmogenic right ventricular dysplasia (ARVD) occurring in the pediatric age group are described. One of the subjects, at the age of 7 years, is believed to be the youngest child in whom ARVD has been diagnosed at autopsy. The clinical and pathological characteristics of ARVD are discussed.

PMID:: 7855018; [PubMed - indexed for MEDLINE]

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The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14.
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Sudden death in childhood due to right ventricular dysplasia: report of two cases.

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