Multiminicore myopathy
ORPHA:598· ICD-10 G71.2
Definition
A rare hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant, Autosomal recessive
- Age of onset
- Antenatal, Childhood, Infancy, Neonatal