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Article

Epidermolytic Ichthyosis Sine Epidermolysis.

The American Journal of dermatopathology - 1 Jun 2017

Eskin-Schwartz Marina, Drozhdina Marianna, Sarig Ofer, Gat Andrea, Jackman Tomer, Isakov Ofer, Shomron Noam, Samuelov Liat, Malchin Natalia, Peled Alon, Vodo Dan, Hovnanian Alain, Ruzicka Thomas, Koshkin Sergei, Harmon Robert M, Koetsier Jennifer L, Green Kathleen J, Paller Amy S, Sprecher Eli

Abstract excerpt

Epidermolytic ichthyosis (EI) is a rare disorder of cornification caused by mutations in KRT1 and KRT10, encoding two suprabasal epidermal keratins. Because of the variable clinical features and severity of the disease, histopathology is often required to correctly direct the molecular analysis. EI is characterized by hyperkeratosis and vacuolar degeneration of the upper epidermis, also known as epidermolytic...

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Source

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Identifiers

PMID: 28121638
DOI: 10.1097/DAD.0000000000000674
PMCID: PMC5489912

Genes

KRT1
KRT10

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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