ORPHA:263553
Peeling skin syndrome type B
Also called Generalized peeling skin disease type B, Generalized peeling skin syndrome type B, Inflammatory peeling skin disease, Inflammatory peeling skin syndrome, PSS type B, PSS1, Peeling skin syndrome 1
- 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:263553 is classified under "Skin diseases" in the Orphanet nomenclature.