Progressive Muscular Atrophy
نویسنده
چکیده
a crack-like ulceration at the junction of the skin and mucous membrane in the two sides of the nose alternately?recurrent attacks of these two complainta during JDecember-January last in a case of progressive muscular atrophy was treated and cured with Bi, plunocaine and sulfanilamide mixed with honey. Was it correct to think that these troubles were of a trophic origin ? As to the P.M.A. the case may be described aa follows : Vague pains in the left arm were felt during the winter of 1945. He (about 60 years) was used to
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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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Spinal muscular atrophy (SMA) is a neuromuscular disorder characterized by degeneration of alpha motor neurons resulting in hypotonia, progressive muscular weakness and atrophy.30 Spinal muscular atrophy is one of the leading hereditary causes of infant mortality,31 it comprises the second most common fatal progressive diseases after cystic fibrosis.28 Spinal muscular atrophy is the most common...
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A Japanese family with progressive spinal muscular atrophy is presented. Seven members in two generations were affected and the mode of inheritance was probably an autosomal recessive trait. A characteristic feature of this family was the presence of oculopharyngeal involvement in some of the affected members, in addition to the variable distribution of muscular atrophy among each of the affect...
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