Peroneal muscular atrophy with pyramidal features.
نویسندگان
چکیده
منابع مشابه
Peroneal muscular atrophy with pyramidal features.
Twenty-five cases of peroneal muscular atrophy with pyramidal features from 15 families are described. This disorder has been referred to as hereditary motor and sensory neuropathy (HMSN) type V by Dyck. Onset was usually in the first two decades of life with difficulty in walking. The clinical syndrome superficially resembled that of HMSN types I and II with distal wasting and weakness involvi...
متن کاملComplete heart block in patients with peroneal muscular atrophy.
Two patients with peroneal muscular atrophy who also had complete heart block are reported. The pathogenesis of heart block in one of these patients was investigated by left ventricular volume analysis which showed a normal ejection fraction, indicating intact left ventricular function. This patient in addition had a normal coronary arteriogram. These findings suggest that heart block in patien...
متن کاملPathology of peroneal muscular atrophy (Charcot-Marie-Tooth disease).
Four cases of peroneal muscular atrophy (Charcot-Marie-Tooth disease) are described in which observations were made from the necropsy examination of the central nervous system, the peripheral nervous system, and the skeletal muscles. The pattern of nerve degeneration in these various locations is described and the conclusion is drawn that the basis of the disease is a very chronic progressive n...
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To render fully intelligible the complete significance of the illustrations, a brief abstract of the notes upon this case must be given :? E. G., aged 22, single, formerly a domestic servant, was admitted to the Bristol Royal Infirmary on March 2nd, 1899. Family History.?Father is of a nervous disposition; one sister is-also nervous, and another suffered for a long time in childhood from a mala...
متن کاملPeroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred.
A large family with autosomal dominant inheritance of peroneal muscular atrophy, associated with extensor plantar responses in some cases, has been studied. Onset was usually in the first two decades and spasticity was not a feature. Nerve conduction studies in 21 cases and light and electron microscope findings on six sural nerve biopsies were similar to those in hereditary motor and sensory n...
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ژورنال
عنوان ژورنال: Journal of Neurology, Neurosurgery & Psychiatry
سال: 1984
ISSN: 0022-3050
DOI: 10.1136/jnnp.47.2.168