Typical nemaline myopathy

MONDO:0015737

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

Also known as: typical congenital nemaline myopathy

4 clinical trials for this condition and its sub-types, 0 tagged with Typical 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 tropomyosin (4) ↑ 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 Typical nemaline myopathy

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

Including sub-types (4) Tagged with Typical nemaline myopathy (0)

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