Phenotypes for disease #05656 (LGMDD4;LGMD1I (dystrophy, muscular, limb-girdle, autosomal dominant, type 4 (LGMDD-4, LGMD-1I)), OMIM:618129)

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0000337378 Limb-girdle muscular dystrophy LGMDD4 see paper; ..., 57y-myalgia thighs, elevated circulating creatine kinase concentration (HP:0003236) 2000 U/L; 60y-waddling gait, CK level 5000 U/L; myopathy (HP:0003198), centrally nucleated skeletal muscle fibers (HP:0003687), proximal muscle weakness (HP:0003701) Unknown 66yy - - WB near absent CAPN3 Camille Verebi 00448143
0000337562 limb‑girdle muscular dystrophy LGMDD4 see paper; ..., 8y-slow, progressive weakness muscles, abnormal gait; 10y-slow, progressive weakness lower limbs, frequent falls, difficulty in standing, walking and climbing stairs; 16y-only walk unaided for <15 min, unable to raise arms above head, no sensory/ocular/bulbar abnormalities, severe weakness proximal muscles all limbs, pelvic and shoulder girdles; 16y-normal mental status, no oculomotor/facial abnormalities with sensory and coordination examinations also finding no abnormalities Familial, autosomal dominant 16y - - - Johan den Dunnen 00448369
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