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Nemaline myopathy

Nemaline myopathy (NM) encompasses a large spectrum of myopathies characterized by hypotonia, weakness and depressed or absent deep tendon reflexes, with pathologic evidence of nemaline bodies (rods) on muscle biopsy.

13 trials tagged with this condition →

Nemaline myopathy 5 2 trials
Childhood-onset nemaline myopathy 1 trial · 2 incl. sub-types Sub-types →
Severe congenital nemaline myopathy 0 trials · 1 incl. sub-types Sub-types →
MYPN-related myopathy 0 trials
Adult-onset nemaline myopathy 0 trials
Nemaline myopathy 5B, autosomal recessive, childhood-onset 0 trials
Nemaline myopathy 5C, autosomal dominant 0 trials
Typical nemaline myopathy 0 trials Sub-types →