ORPHA:486
Autosomal dominant severe congenital neutropenia
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Europe)
- Rarity class
- <1 / 1 000 000
ORPHA:486 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Recurrent bacterial infections
- Recurrent viral infections
- Oral ulcer
- Gingivitis
- Periodontitis
- Recurrent skin infections