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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

38 clinical trials for this condition and its sub-types.

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Sub-types

Nemaline myopathy 8 (1) Congenital myopathy 2a, typical, autosomal dominant (0) Nemaline myopathy 10 (0) Nemaline myopathy 2 (0) Nemaline myopathy 9 (0)

Broader categories

Disease (618) Nervous system disorder (217) Musculoskeletal system disorder (196) Hereditary disease (172) Muscle tissue disorder (53) Human disease (14) Nemaline myopathy (13) Myopathy (11) Congenital myopathy (8) Skeletal muscle disorder (8)
Trials to join now! 19 Not yet recruiting 7 Not yet finished but already full! 4 Completed 7 Terminated 1
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