ORPHA:817
Peeling skin syndrome
Also called Deciduous skin, Familial continuous skin peeling syndrome, Idiopathic deciduous skin, Keratosis exfoliativa congenita, PSS, Peeling skin disease
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:817 is classified under "Skin diseases" in the Orphanet nomenclature.