DefinitionThis section has been translated automatically.
Rare form of keratinopathic ichthyosis with transient, sickle-shaped, circulatory or anular reddish hyperkeratotic plaques.
EtiopathogenesisThis section has been translated automatically.
This is caused by mutations in the genes keratin-1 and keratin-10. It is probably a minus variant of superficial epidermolytic ichthyosis (Jha A et al. 2015).
HistologyThis section has been translated automatically.
LiteratureThis section has been translated automatically.
- Jha A et al (2015) Annular epidermolytic ichthyosis: a rare phenotypic variant of bullous congenital ichthyosiform erythroderma. Indian J Dermatol Venereol Leprol 81:194-197.
- Yoneda K et al (1999) Annular epidermolytic ichthyosis. Br J Dermatol 141:748-750. Review.
- Zaki TDet al. (2018) A p.478I>T KRT1 mutation in a case of annular epidermolytic ichthyosis. Pediatric Dermatol 35:e414-e415.
Outgoing links (1)Superficial epidermolytic ichthyosis;
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