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Mitochondrial myopathy presenting as ataxia with dilated cardiomyopathy.
Indian J Pediatr ; 2001 Apr; 68(4): 347-50
Article in English | IMSEAR | ID: sea-83501
ABSTRACT
Mitochondrial disorders are multisystem diseases with very heterogeneous clinical manifestations. Common cardiac features include cardiomyopathy and conduction defects. We report a five-year-old boy who presented with signs of congestive cardiac failure and was diagnosed to have dilated cardiomyopathy. Six months later, he developed progressively worsening ataxia, hypotonia, other cerebellar signs, hearing loss, severe sensory peripheral neuropathy and lactic acidosis. Electronmicroscopy of skeletal muscle biopsy was consistent with mitochondrial myopathy.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Ataxia / Humans / Male / Microscopy, Electron / Cardiomyopathy, Dilated / Child, Preschool / Mitochondrial Myopathies / Diagnosis, Differential Type of study: Diagnostic study Language: English Journal: Indian J Pediatr Year: 2001 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Ataxia / Humans / Male / Microscopy, Electron / Cardiomyopathy, Dilated / Child, Preschool / Mitochondrial Myopathies / Diagnosis, Differential Type of study: Diagnostic study Language: English Journal: Indian J Pediatr Year: 2001 Type: Article