Rare Zebra

Rare disease search prototype built on Orphanet data

← Back to search

ORPHA:263534

Acral peeling skin syndrome

Also called Acral PSS, Localized PSS, PSS 2, Peeling skin syndrome 2

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:263534 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Eczematoid dermatitis
  • Ichthyosis
  • Abnormal blistering of the skin
  • High hypermetropia
  • Erythema
  • Allergy