Синдром CINCA
ORPHA:1451· ICD-10 E85.0· CINCA syndrome
Визначення(English summary)
A rare, genetic, cryopyrin-associated periodic syndrome (CAPS) characterized by neonatal onset of systemic inflammation, urticarial skin rash and arthritis/arthralgia resulting in severe arthropathy and central nervous system involvement (including chronic aseptic meningitis, brain atrophy and sensorineural hearing loss).
- Поширеність
- Unknown
- Успадкування
- Autosomal dominant, Not applicable
- Вік початку
- Infancy, Neonatal