Myasthenische Syndrome, kongenitale, mit Glykosylierungsdefekt
ORPHA:353327· ICD-10 G70.2· Congenital myasthenic syndrome with glycosylation defect
- Prävalenz
- Unknown
- Vererbung
- Autosomal recessive
- Erkrankungsalter
- Infancy, Neonatal
ORPHA:353327· ICD-10 G70.2· Congenital myasthenic syndrome with glycosylation defect