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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.

5 trials tagged with this condition →

This condition has no sub-types.