Amish nemaline myopathy
ORPHA:98902· ICD-10 G71.2
Definition
A type of nemaline myopathy (NM) only observed in several families of the Amish community.
- Prevalence
- >1 / 1000
- Inheritance
- Autosomal recessive
- Age of onset
- Neonatal
ORPHA:98902· ICD-10 G71.2
A type of nemaline myopathy (NM) only observed in several families of the Amish community.