The Retinal Manifestations of Mitochondrial Myopathy
- 1 December 1985
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 103 (12) , 1825-1830
- https://doi.org/10.1001/archopht.1985.01050120059020
Abstract
• In a series of 61 patients with the morphologic and histochemical features of mitochondrial myopathy, 22 (36%) had pigmentary retinopathy. Three patterns of retinopathy were identified. Eighteen patients had a "salt and pepper" type of retinal appearance, which was usually associated with good visual function. Two had many features of retinitis pigmentosa, and two others showed generalized loss, or atrophy, of the retinal pigment epithelium and choriocapillaris. These last four patients had markedly reduced visual acuities, with optic atrophy and attenuated retinal vessels. Electroretinography and electro-oculography were performed in 11 patients. Both rod and cone mediated electroretinographic functions were subnormal in eight patients, while only cone mediated functions were depressed in the remaining three. The electro-oculographic changes were variable.This publication has 4 references indexed in Scilit:
- THE CLINICAL FEATURES OF MITOCHONDRIAL MYOPATHYBrain, 1986
- Retinal pathology in the Kearns-Sayre syndrome.British Journal of Ophthalmology, 1985
- The Atypical Pigmentary Retinopathy of Kearns-Sayre SyndromeOphthalmology, 1982
- Origin and sensitivity of the light peak in the intact cat eyeThe Journal of Physiology, 1982