atrofie spinálne svalové, infantilný a juvenilný typ
Subject h.
atrofie spinálne svalové, infantilný a juvenilný typ
Subject h.
Spinal Muscular Atrophies of Childhood
Entry terms
atrofie spinálne svalové detské atrofie spinálne svalové, v detstve atrofia spinálna muskulárna, infantilný typ atrofia spinálna muskulárna, juvenilný typ Werdnigova-Hoffmannova choroba atrophia spinalis progressiva infantilis HMN proximálny typ I atrofia svalová spinálna detská Kugelbergova-Welanderovej choroba atrofia spinálna svalová juvenilná
Scope note in English
A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)
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(2) - CiBaMed
subject heading
Number of the records: 1
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