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Up to: Familial cardiomyopathy · Mitochondrial oxidative phosphorylation disorder · Inborn mitochondrial myopathy

Fatal infantile encephalocardiomyopathy

Fatal infantile cytochrome C oxidase deficiency is a very rare mitochondrial disease characterized clinically by cardioencephalomyopathy resulting in death in infancy.

0 trials tagged with this condition →

  • Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 0 trials
  • Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 0 trials
  • Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 0 trials
  • Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 0 trials

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