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scapuloperoneal myopathy (scapuloperoneal syndrome myopathic type)
Genetics:
- associated with defects in MYH7
- X-linked dominant form associated with defects in FHL1
Clinical manifestations:
- progressive myopathy beginning in the lower legs & affecting the shoulder region earlier & more severely than distal arm
General
genetic disease of muscle (inherited myopathy)
Database Correlations
OMIM correlations
References
OMIM :accession 181430