[Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children].
D001284:Atrophy; D002648:Child; D040941:Heredity; D006801:Humans; D009133:Muscular Atrophy; D009134:Muscular Atrophy, Spinal; D009468:Neuromuscular Diseases; D014897:Spinal Muscular Atrophies of Childhood
AMYOTONIA CONGENITA; ATROPHY, MUSCULAR
Atrophia progressiva musculorum infantum (Werdnig-Hoffmann); klinik, patologi, arvelighedsfaktorer, og forhold til amyotonia congenita (Oppenheim) og andre lede- resp. muskelatoniformer hos børn.