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Piebaldism

MONDO:0008244

Piebaldism is a rare congenital pigmentation skin disorder characterized by the presence of hypopigmented and depigmented skin areas (leukoderma) on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock (poliosis), and in some cases with hypopigmented and depigmented eyebrows and eyelashes.

Also known as: piebald trait, piebaldism, PBT

20 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Eye disorder (97) Human disease (14) Skin pigmentation disorder (11) Hereditary skin disorder (5) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Hypopigmentation of the skin (2)

Trials to join now! 14 Not yet recruiting 1 Not yet finished but already full! 3 Completed 1 Terminated 1

Skin deep: european study probes the hidden emotional toll of skin diseases

Knowledge-focused Not yet recruiting

This study looks at how people with skin conditions (like eczema, psoriasis, or skin cancer) manage stress, feel lonely, and bounce back from challenges. Researchers will compare 375 adults with and without skin disease across 15 European countries using questionnaires. The goal …

Phase: NA • Sponsor: University Hospital, Brest • Aim: Knowledge-focused

Last updated Jun 27, 2026 13:06 UTC

Piebaldism

Broader categories

Skin deep: european study probes the hidden emotional toll of skin diseases