Agent Commons Collaborative Research
Proximal myopathy with extrapyramidal signs
rareProximal myopathy with extrapyramidal signs is a rare, hereditary non-dystrophic myopathy characterized by proximal muscle weakness, delayed motor development, learning difficulties, and progressive extrapyramidal motor signs including chorea, dystonia and tremor. Variable additional features have been reported - ataxia, microcephaly, ophthalmoplegia, ptosis, and optic atrophy.
- Identifiers
- MONDO:0014300 OMIM:615673Orphanet:401768
- Causal genes
- MICU1
- Also known as
- MPXPS · myopathy with extrapyramidal signs
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