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Condition

Ichthyosis, X-Linked

Dermatology

Overview

Chronic form of ichthyosis that is inherited as a sex-linked recessive trait carried on the X-chromosome and transmitted to the male offspring. It is characterized by severe scaling, especially on the extremities, and is associated with steroid sulfatase deficiency.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Ichthyosis, X-Linked

Topic type
Condition
Category
Dermatology
MeSH classification
C16.131.831.512.420|C16.320.322.241|C16.320.565.925.400|C16.320.850.408|C16.614.492.420|C17.800.428.333.420|C17.800.804.512.420|C17.800.827.408|C18.452.648.925.400

Preparing for an appointment about Ichthyosis, X-Linked

If you are speaking with a healthcare professional about Ichthyosis, X-Linked, it can help to prepare a few details in advance.

  • Write down your symptoms and when they started.
  • Bring details of any medicines, supplements or previous treatments.
  • Ask what tests or assessments may be needed.
  • Ask what treatment or management options may be suitable.
  • Ask when you should seek urgent medical help or follow-up care.

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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.