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Up to: Developmental defect during embryogenesis · Hereditary skin disorder · Hyperpigmentation of the skin · Noonan syndrome and Noonan-related syndrome
Legius syndrome
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.
This condition has no sub-types.