Charcot-Marie-Tooth disease with leber optic atrophy

J. G. McLeod, D. Phil, P. A. Low, J. A. Morgan

Research output: Contribution to journalArticle

35 Scopus citations

Abstract

A family is described in which visual failure was associated with hypertrophic Charcot-Marie-Tooth disease. The diagnosis of Charcot-Marie-Tooth disease was confirmed by electrophysiologic studies and by quantitative histologic studies of sural nerve biopsies. The clinical features and mode of inheritance of the visual failure were those of Leber optic atrophy. The two conditions were inherited independently.

Original languageEnglish (US)
Pages (from-to)179-184
Number of pages6
JournalNeurology
Volume28
Issue number2
StatePublished - Feb 1978

ASJC Scopus subject areas

  • Clinical Neurology

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  • Cite this

    McLeod, J. G., Phil, D., Low, P. A., & Morgan, J. A. (1978). Charcot-Marie-Tooth disease with leber optic atrophy. Neurology, 28(2), 179-184.