Recessive X-linked ichthyosis
ORPHA:461· ICD-10 Q80.1
Definition
A rare genetic skin disease belonging to the Mendelian Disorders of Cornification (MeDOC) and characterized by generalized hyperkeratosis and scaling of the skin. The condition is rather mild.
- Prevalence
- 1-5 / 10 000
- Inheritance
- X-linked recessive
- Age of onset
- Neonatal