All individuals with variants in gene CHCHD10

2 entries on 1 page. Showing entries 1 - 2.
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00143201 - - - M - (Germany) - - - - - ? Parkinsonism (HP:0001300); Bradykinesia (HP:0002067); Intention tremor (HP:0002080) 1 1 IMGAG
00473751 Fam9609464Pat1202 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history F no Iran - - - - - NMD onset 33 y/o with Lt. foot weakness; Nasal speech; Fatigue while long distance walking, running & climbing steps; Neck weakness; Muscle weakness, proximal, legs; Foot drop, mild, bilateral; Abnormal gait, mild; Difficulty rising from seated position. Muscle biopsy revealed rimmed vacuole myopathy with prominent disruption of intermyofibrillar network pattern as wiped-out fibers and cytoplasmic core-like lesions. EMG-NCV findings are compatible with partial ant horn cell disease. 1 1 Johan den Dunnen
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