ORPHA:79394
Congenital ichthyosiform erythroderma
Also called CIE, Erythrodermic ichthyosis, Non-bullous congenital ichthyosiform erythroderma
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- 1-9 / 1 000 000 (Spain)
- Rarity class
- 1-9 / 1 000 000
ORPHA:79394 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Ectropion
- Hypohidrosis
- Pruritus
- Erythroderma
- Ichthyosis
- Hearing impairment