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