Literature DB >> 3587632

Cardiomyopathy, mental retardation, and autophagic vacuolar myopathy.

Z H Hart, S Servidei, P L Peterson, C H Chang, S DiMauro.   

Abstract

Two brothers had nonobstructive hypertrophic cardiomyopathy, mental retardation, and vacuolar myopathy, and their mother died of cardiopathy at age 31. Seven families with this syndrome have been described; heredity appears to be X-linked dominant or autosomal dominant, with different expressivity in males and females. The biochemical cause of this lysosomal storage disease is unknown.

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Year:  1987        PMID: 3587632     DOI: 10.1212/wnl.37.6.1065

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

Review 1.  Primary lipid cardiomyopathy.

Authors:  A Zimmermann; P Wyss; F Stocker
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

2.  Familial X-linked cardiomyopathy (Danon disease): diagnostic confirmation by mutation analysis of the LAMP2gene.

Authors:  Christian Balmer; Diana Ballhausen; Nils U Bosshard; Beat Steinmann; Eugen Boltshauser; Urs Bauersfeld; Andrea Superti-Furga
Journal:  Eur J Pediatr       Date:  2005-05-12       Impact factor: 3.183

3.  Danon disease: case report and detection of new mutation.

Authors:  G Regelsberger; R Höftberger; W F Pickl; G J Zlabinger; U Körmöczi; U Salzer-Muhar; D Luckner; O A Bodamer; J A Mayr; W H Muss; H Budka; H Bernheimer
Journal:  J Inherit Metab Dis       Date:  2009-07-07       Impact factor: 4.982

  3 in total

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