Peroneal Muscular Atrophy

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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...

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Pathology 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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Complete 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...

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A Case of Neuritic Muscular Atrophy ("Peroneal" Type)

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...

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Spinal Muscular Atrophy: A Short Review Article

Spinal muscular atrophy (SMA) is a genetic disorder which affect nervous system and is characterized with progressive distal motor neuron weakness. The survival motor neuron (SMN) protein level reduces in patients with SMA. Two different genes code survival motor neuron protein in human genome. Skeletal and intercostal muscles denervation lead to weakness, hypotony, hyporeflexia, respiratory fa...

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ژورنال

عنوان ژورنال: Proceedings of the Royal Society of Medicine

سال: 1934

ISSN: 0035-9157

DOI: 10.1177/003591573402701019