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Article

Revisiting X-linked congenital ichthyosis.

International journal of dermatology - 1 Jan 2025

Zhou Baishun, Liang Cancan, Li Peiyao, Xiao Heng

Abstract excerpt

X-linked recessive ichthyosis (XLI) is a hereditary skin disease characterized by generalized dryness and scaling of the skin, with frequent extracutaneous manifestations. It is the second most common type of ichthyosis, with a prevalence of 1/6,000 to 1/2,000 in males and without any racial or geographical differences. The causative gene for XLI is the steroid sulfatase gene (STS), located on Xp22.3. STS...

Topics

Humans
Ichthyosis, X-Linked
Steryl-Sulfatase
Diagnosis, Differential
Mutation
Epidermis

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 39086014
DOI: 10.1111/ijd.17396

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