ORPHA:263548
Peeling skin syndrome type A
Also called Generalized peeling skin syndrome type A, Non-inflammatory generalized peeling skin syndrome type A., Non-inflammatory peeling skin syndrome type A, PSS type A
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:263548 is classified under "Skin diseases" in the Orphanet nomenclature.