Nemaline myopathy
MONDO:0018958Nemaline 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.
Also known as: NEM, NM, nemaline body disease, nemaline myopathy, nemaline rod myopathy, rod myopathy, Rod body disease, Rod-body myopathy
17 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Nemaline myopathy 5
(2)
Childhood-onset nemaline myopathy
(1)
Nemaline myopathy 6
(1)
Nemaline myopathy 8
(1)
Adult-onset nemaline myopathy
(0)
Congenital myopathy 23
(0)
Congenital myopathy 2a, typical, autosomal dominant
(0)
Congenital myopathy 4B, autosomal recessive
(0)
MYPN-related myopathy
(0)
Nemaline myopathy 10
(0)
Nemaline myopathy 2
(0)
Nemaline myopathy 5B, autosomal recessive, childhood-onset
(0)
Nemaline myopathy 5C, autosomal dominant
(0)
Nemaline myopathy 7
(0)
Nemaline myopathy 9
(0)
Severe congenital nemaline myopathy
(0)
Typical nemaline myopathy
(0)