Congenital myasthenic syndrome
What is Congenital myasthenic syndrome?
Congenital myasthenic syndrome (CMS) is a group of genetic disorders of impaired neuromuscular transmission at the motor endplate characterized by fatigable muscle weakness.
Other condition names
- CMS
Inheritance type
Autosomal dominant, Autosomal recessive
Prevalence
- Europe: 1-9 in 1,000 000
Age of Onset
- Infancy
- Neonatal
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