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

Severe congenital nemaline myopathy

Severe congenital nemaline myopathy is a severe form of nemaline myopathy (NM) characterized by severe hypotonia with little spontaneous movement in neonates.

0 trials tagged with this condition →

  • Nemaline myopathy 8 1 trial
  • Congenital myopathy 2a, typical, autosomal dominant 0 trials
  • Nemaline myopathy 10 0 trials
  • Nemaline myopathy 2 0 trials
  • Nemaline myopathy 9 0 trials

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