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Legius syndrome

MONDO:0012669

Legius syndrome, also known as NF1-like syndrome, is a rare, genetic skin pigmentation disorder characterized by multiple cafC)-au-lait macules with or without axillary or inguinal freckling.

Also known as: Legius syndrome, NF1-like syndrome, neurofibromatosis 1-like syndrome, neurofibromatosis type 1 like syndrome, neurofibromatosis type 1-like syndrome

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

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Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Musculoskeletal system disorder (207) Hereditary disease (176) Cardiomyopathy (144) Skin disorder (132) Hypertrophic cardiomyopathy (112) Muscle tissue disorder (56) Intrinsic cardiomyopathy (16)
Trials to join now! 9 Not yet recruiting 1 Not yet finished but already full! 2 Completed 2
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  • Could you help scientists unlock genetic cancer secrets?

    Knowledge-focused Not yet recruiting

    This study screens up to 1,000 people with personal or family histories of certain cancers to see if they qualify for ongoing genetics research at the National Cancer Institute. Participants fill out a 15-20 minute online survey about their health and family history. No treatment…

    Sponsor: National Cancer Institute (NCI) • Aim: Knowledge-focused

    Last updated Aug 18, 2026 06:00 UTC

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