ORPHA:98905
Congenital multicore myopathy with external ophthalmoplegia
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:98905 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- External ophthalmoplegia
- Motor delay
- Generalized hypotonia
- Muscle weakness
- Decreased fetal movement
- Myopathic facies