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Kugelberg-Welander s. a hereditary form of spinal muscular atrophy, usually transmitted as an autosomal recessive trait, due to lesions of the anterior horns of the spinal cord. Onset is in the first or second decade, principally between two and seventeen years, with atrophy and weakness of the proximal muscles of the lower extremities and pelvic girdle, followed by involvement of the distal muscles and muscular twitchings. Cf. Werdnig-Hoffmann spinal muscular atrophy. Called also juvenile or proximal spinal muscular atrophy and Wohlfart-Kugelberg-Welander s.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
Kugelberg-Welander syndrome see under syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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