Infantile

Subacute necrotizing encephalopathy or Leigh's disease (I, II) Progressive infantile poliodystrophy or Alpers' disease (IV) Lethal infantile mitochondrial disease (I) Others

Hypertrophic cardiomyopathy and myopathy (II)

Infantile bilateral striatal necrosis and Leber's hereditary optic neuropathy ( II ) Mitochondrial myopathies (I)

Benign infantile mitochondrial myopathy and cardiomyopathy (I) Lethal infantile cardiomyopathy, X-linked or Barth's syndrome (I) Benign infantile mitochondrial myopathy (I) CHILDHOOD

Myoclonic epilepsy and ragged red fiber disease (II)

Mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (II) Chronic progressive external ophthalmoplegia, autosomal dominant (I) Kearns-Sayre syndrome, autosomal dominant (I) Others

Mitochondrial myopathy (II, IV) Idiopathic dystonia (IV)

Myoneurogastrointestinal disorder and encephalopathy (IV)

Lufts disease (nonthyroid hypermetabolism) with generalized myopathy (IV)

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