Original article
English
K. Radhakrishnan 1, R. Sridharan 1, P.P. Ashok 1, M.A. Elmangoush 2
1-Division of Neurology, Department of Medicine, Faculty of Medicine, University of Garyounis, Benghazi, S.P.L.A.J. 2-Department of Medicine, Faculty of Medicine, University of Garyounis, Benghazi, S.P.L.A.J.
Garyounis Medical Journal Vol. 8, No.1. July 1984: 45-48
Abstract
Ten members of a Libyan family with peroneal muscular atrophy (hereditary motor and sensory neuropathy) are reported. The clinical and electrophysiological features favoured type I disease. Tile pedigree of tile family revealed an autosomal dominant inheritance pattern. The clinical, genetic, and electrophysiological basis for the classification of this disease is discussed.
Keywords: Charcot-Marie-Tooth Disease (Hereditary Motor and Sensory Neuropathy)
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