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Hereditary poikiloderma

MONDO:0016382

1 clinical trial for this condition and its sub-types.

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Sub-types

Hereditary sclerosing poikiloderma, Weary type (0) Hereditary sclerosing poikiloderma with tendon and pulmonary involvement (0) Inflammatory poikiloderma with hair abnormalities and acral keratoses (0) Poikiloderma with neutropenia (0)

Broader categories

Disease (717) Skin disorder (135) Human disease (15) Disease by body system or component (0) Epidermal disease (0) Integumentary system disorder (0)

Genetic sleuths hunt for hidden causes of rare skin disorder

Knowledge-focused Completed

This study used advanced genetic sequencing to find new genes responsible for syndromic poikiloderma, a rare condition affecting skin and other organs. Researchers analyzed DNA from 39 patients to improve diagnosis, genetic counseling, and tumor risk monitoring. The goal is to he…

Sponsor: Centre Hospitalier Universitaire Dijon • Aim: Knowledge-focused

Last updated Jun 27, 2026 11:01 UTC