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Q J Med 1990; 74: 41-48
© 1990 Association of Physicians

other

Endocrine Aspects of Mitochondrial Cytopathy: Marked Phenotypic Variation in Two Affected Siblings

LOUIS HERZBERG

University Department of Medicine, Repatriation Hospital Nedlands, Western Australia

Accepted for publication 24 July 1989.

Two siblings with ‘mitochondrial myopathy’, one of whom was found to have hypergonado-trophic hypogonadism whilst the other had normal endocrine function are reported. The inheritance suggests an autosomal recessive mode. The protean manifestations of the disorder are emphasized. Attention is drawn to the possible association of endocrine abnormalities in addition to the more widely recognized neuromuscular signs.


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