Legius Syndrome - an overview

Multiple café-au-lait macules and movement disorder: think beyond neurofibromatosis

Syndromes The RASopathies Network

SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype

Frontiers Novel pathogenic variants in KIT gene in three Chinese piebaldism patients

Cureus, Legius Syndrome and Inflammatory Bowel Disease: A Pediatric Case Report

Café-au-lait macule differential by craniofacial examination. Many of

Neurofibromatosis type I - Wikipedia

Noonan syndrome: MedlinePlus Genetics

DermNet - New page - Legius syndrome: a rare disorder characterised by café-au-lait macules. Read more

Changing facial phenotype in Cohen syndrome: towards clues for an earlier diagnosis

Lisch nodules and iris mammillations in two siblings with familial legius syndrome - Bixel - 2020 - Clinical Case Reports - Wiley Online Library

Café‐au‐lait macules and intertriginous freckling in piebaldism: Clinical overlap with neurofibromatosis type 1 and Legius syndrome - Stevens - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library

Society for Pediatric Anesthesia - SPA News