Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C>T diagnosed in an adult male.

Abstract:

:Mitochondrial disorders comprise a heterogeneous group of diseases with multisystem involvement including myocardium. Most cases of mitochondrial cardiomyopathy are associated with myopathy and encephalopathy and are generally present in infancy or childhood. The disease often exhibits a rapid downward course with death frequently occuring within the first year of life. We describe a unique case of hypertrophic cardiomyopathy due to mitochondrial DNA mutation m.3303C >T in the MT-TL1 gene, diagnosed accidentally in a 35-year-old male. The patient initially presented with stroke of assumed cardioembolic origin due to the presence of two interatrial communications associated with mobile aneurysm of the interatrial septum. No other extracardiac manifestations of mitochondrial disorder were observed.

journal_name

Int Heart J

authors

Palecek T,Tesarova M,Kuchynka P,Dytrych V,Elleder M,Hulkova H,Hansikova H,Honzik T,Zeman J,Linhart A

doi

10.1536/ihj.53.383

subject

Has Abstract

pub_date

2012-01-01 00:00:00

pages

383-7

issue

6

eissn

1349-2365

issn

1349-3299

pii

DN/JST.JSTAGE/ihj/53.383

journal_volume

53

pub_type

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