ORPHA:461
Recessive X-linked ichthyosis
Also called RXLI, Steroid sulfatase deficiency, X-linked ichthyosis, XLI
- Body system
- Skin diseases
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Neonatal
- Estimated prevalence
- 1-5 / 10 000 (Europe)
- Rarity class
- 1-5 / 10 000
ORPHA:461 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Dry skin
- Hyperkeratosis
- Hypohidrosis
- Ichthyosis
- Attention deficit hyperactivity disorder
- Opacification of the corneal stroma