[Two cases of familial congenital muscular dystrophy simulating Werdnig-Hoffman-Oppenheim disease].
D003937:Diagnosis, Differential; D006801:Humans; D009134:Muscular Atrophy, Spinal / Q000175:diagnosis*; D009136:Muscular Dystrophies / Q000175:diagnosis*; D049288:Muscular Dystrophies, Limb-Girdle; D014897:Spinal Muscular Atrophies of Childhood
PROGRESSIVE MUSCULAR ATROPHY/differential diagnosis; PROGRESSIVE MUSCULAR DYSTROPHY/differential diagnosis
Deux cas de dystrophie musculaire familiale congénitale simulant une maladie de Werdnig-Hoffmann-Oppenheim.