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Congenital nemaline myopathy
- ... 6; NEM6 CONGENITAL MYOPATHY 4B, AUTOSOMAL RECESSIVE; CMYO4B CONGENITAL MYOPATHY 23; CMYO23 NEMALINE MYOPATHY 8; NEM8 NEMALINE MYOPATHY 9; NEM9 NEMALINE ...
- ... their family. Actin filament aggregate myopathy Actin myopathy Congenital myopathy with excess of thin filaments Nemaline myopathy 3 Genetic Testing Registry: Actin accumulation myopathy ...
- ... disorder in their family. Intranuclear nemaline rod myopathy Nemaline myopathy with exclusively intranuclear rods Genetic Testing Registry: Actin accumulation myopathy National Organization for Rare Disorders (NORD) CONGENITAL MYOPATHY 2A, TYPICAL, AUTOSOMAL DOMINANT; CMYO2A PubMed Feng ...
- Cap myopathy is a disorder that primarily affects skeletal muscles, which are muscles that the body uses for movement. People with cap myopathy have muscle ...