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Up to: Hereditary neurological disease · Neuromuscular disease caused by qualitative or quantitative defects of selenoprotein N1

Multiminicore myopathy

A hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy.

1 trial tagged with this condition →

Rigid spine muscular dystrophy 1 1 trial Sub-types →
Antenatal multiminicore disease with arthrogryposis multiplex congenita 0 trials
Classic multiminicore myopathy 0 trials
Congenital multicore myopathy with external ophthalmoplegia 0 trials
Moderate multiminicore disease with hand involvement 0 trials