Severe congenital nemaline myopathy

MONDO:0015735

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

Also known as: severe congenital (neonatal) NM

5 clinical trials for this condition and its sub-types, 0 tagged with Severe congenital nemaline myopathy itself.

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↑ Hereditary neurological disease (5791) ↑ Congenital nervous system disorder (287) ↑ Nemaline myopathy (13) ↑ Neuromuscular disease caused by qualitative or quantitative defects of alpha-actin (2) ↑ Neuromuscular disease caused by qualitative or quantitative defects of nebulin (2)

Sub-types of Severe congenital nemaline myopathy

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

Including sub-types (5) Tagged with Severe congenital nemaline myopathy (0)

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