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Up to: Hereditary neurological disease · Congenital nervous system disorder · Nemaline myopathy · Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin · Neuromuscular disease caused by qualitative or quantitative defects of alpha-actin · Neuromuscular disease caused by qualitative or quantitative defects of nebulin

Typical nemaline myopathy

Typical nemaline myopathy is a moderate neonatal form of nemaline myopathy (NM) characterized by facial and skeletal muscle weakness and mild respiratory involvement.

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Congenital myopathy 23 0 trials
Congenital myopathy 2a, typical, autosomal dominant 0 trials
Nemaline myopathy 10 0 trials
Nemaline myopathy 2 0 trials
Nemaline myopathy 7 0 trials
Nemaline myopathy 9 0 trials