Literature DB >> 7855018

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

B R Pawel1, J P de Chadarévian, J H Wolk, R M Donner, R L Vogel, P Braverman.   

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.

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Year:  1994        PMID： 7855018     DOI： 10.3109/15513819409037695

Source DB:  PubMed          Journal:  Pediatr Pathol        ISSN： 0277-0938


  4 in total

1.  The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14.

Authors:  D Li; F Ahmad; M J Gardner; D Weilbaecher; R Hill; A Karibe; O Gonzalez; T Tapscott; G P Sharratt; L L Bachinski; R Roberts
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Arrhythmogenic right ventricular cardiomyopathy in an 11-year-old girl and typical echocardiographic features.

Authors:  Abdul Rahim Wong; Nabil AbdurRazak; Saad Mohammad Al-Hadlaq; Abdullah Salem Al-Jarallah
Journal:  Pediatr Cardiol       Date:  2007-09-21       Impact factor: 1.655

3.  Is arrhythmogenic right ventricular cardiomyopathy a paediatric problem too?

Authors:  P Turrini; C Basso; L Daliento; A Nava; G Thiene
Journal:  Images Paediatr Cardiol       Date:  2001-01

4.  Arrhythmogenic right ventricular cardiomyopathy with biventricular involvement and heart failure in a 9-year old girl.

Authors:  Fateh Ali Tipoo Sultan; Mehnaz Atiq Ahmed; Jamie Miller; Joseph B Selvanayagam
Journal:  J Saudi Heart Assoc       Date:  2016-08-24
  4 in total

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