Literature DB >> 11370443

Mitochondrial myopathy presenting as ataxia with dilated cardiomyopathy.

S Gulati1, A Das Gupta, M Kabra, R Juneja, M C Sharma, V Kalra.   

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.

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Year:  2001        PMID: 11370443     DOI: 10.1007/bf02721845

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  12 in total

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2.  Mitochondrial mutation in fatal infantile cardiomyopathy.

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Journal:  Lancet       Date:  1990-12-08       Impact factor: 79.321

3.  Reversal of a mitochondrial DNA defect in human skeletal muscle.

Authors:  K M Clark; L A Bindoff; R N Lightowlers; R M Andrews; P G Griffiths; M A Johnson; E J Brierley; D M Turnbull
Journal:  Nat Genet       Date:  1997-07       Impact factor: 38.330

Review 4.  Mitochondrial cardiomyopathy: molecular and biochemical analysis.

Authors:  J Marin-Garcia; M J Goldenthal
Journal:  Pediatr Cardiol       Date:  1997 Jul-Aug       Impact factor: 1.655

5.  Cardiac involvement in mitochondrial diseases, and vice versa.

Authors:  R S Williams
Journal:  Circulation       Date:  1995-02-15       Impact factor: 29.690

Review 6.  Oxidative phosphorylation diseases and mitochondrial DNA mutations: diagnosis and treatment.

Authors:  J M Shoffner; D C Wallace
Journal:  Annu Rev Nutr       Date:  1994       Impact factor: 11.848

Review 7.  Mitochondrial disorders: clinical and genetic features.

Authors:  D K Simon; D R Johns
Journal:  Annu Rev Med       Date:  1999       Impact factor: 13.739

Review 8.  Cardiomyopathy and abnormal mitochondrial function.

Authors:  J Marin-Garcia; M J Goldenthal
Journal:  Cardiovasc Res       Date:  1994-04       Impact factor: 10.787

9.  Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects.

Authors:  R Anan; M Nakagawa; M Miyata; I Higuchi; S Nakao; M Suehara; M Osame; H Tanaka
Journal:  Circulation       Date:  1995-02-15       Impact factor: 29.690

10.  A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.

Authors:  G Silvestri; F M Santorelli; S Shanske; C B Whitley; L A Schimmenti; S A Smith; S DiMauro
Journal:  Hum Mutat       Date:  1994       Impact factor: 4.878

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