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Congenital muscular dystrophy. A case report with autopsyfindings. 1963

J K SHORT

UI MeSH Term Description Entries
D009136 Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. Muscular Dystrophy,Myodystrophica,Myodystrophy,Dystrophies, Muscular,Dystrophy, Muscular,Myodystrophicas,Myodystrophies
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D049288 Muscular Dystrophies, Limb-Girdle A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles). Limb-Girdle Muscular Dystrophies,Limb-Girdle Muscular Dystrophy,Limb-Girdle Syndrome,Muscular Dystrophy, Limb-Girdle,Myopathic Limb-Girdle Syndrome,Limb Girdle Muscular Dystrophies,Limb Girdle Muscular Dystrophy,Muscular Dystrophies, Limb Girdle,Muscular Dystrophy, Limb Girdle

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