Fuch's corneal dystrophy in a patient with mitochondrial DNA mutations

    loading  Checking for direct PDF access through Ovid

Abstract

A patient with Fuch's corneal, dystrophy, sensorineural hearing loss, diabetes, cardiac conduction defects, ataxia, and hyperreflexia is described.Analysis of lymphocyte mitochondrial DNA showed missense mutations usually associated with Leber's hereditary optic neuropathy. The occurrence of Fuch's dystrophy in this patient and the biology of corneal endothelial cells suggest that mitochondrial defects could be the cause of Fuch's endothelial dystrophy.

(J Med Genet 1998;35:258-259)

Related Topics

    loading  Loading Related Articles