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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

Childhood-onset nemaline myopathy

Childhood onset nemaline myopathy, or mild nemaline myopathy is a type of nemaline myopathy (NM) characterized by distal muscle weakness, and sometimes slowness of muscle contraction.

1 trial tagged with this condition →

Nemaline myopathy 6 1 trial
Congenital myopathy 23 0 trials
Congenital myopathy 2a, typical, autosomal dominant 0 trials
Congenital myopathy 4B, autosomal recessive 0 trials
Nemaline myopathy 2 0 trials
Nemaline myopathy 9 0 trials