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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
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  • AI could cut skin specialist wait times, study hints

    Knowledge-focused Completed

    This study tested an artificial intelligence algorithm designed to help primary care doctors decide whether a patient with a skin condition really needs to see a dermatologist. Researchers enrolled 200 adults with skin problems and had their doctors take photos of the affected ar…

    Sponsor: AI Labs Group S.L • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:11 UTC

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