Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:2273

Ichthyosis follicularis-alopecia-photophobia syndrome

Also called IFAP syndrome, Ichthyosis follicularis-atrichia-photophobia syndrome

Body system
Skin diseases
Inheritance pattern
Autosomal dominant, Not applicable, X-linked recessive
Typical age of onset
Infancy, Neonatal
Estimated prevalence
<1 / 1 000 000 (Worldwide)
Rarity class
<1 / 1 000 000

ORPHA:2273 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Photophobia
  • Intellectual disability
  • Seizure
  • Specific learning disability
  • Abnormality of the hair
  • Alopecia