Rare Zebra

Rare disease search prototype built on Orphanet data

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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