Legius Syndrome - an overview

Genetic Clinics

Figure 2 from Legius syndrome, an Update. Molecular pathology of mutations in SPRED1.

Clinical features in 14 families with Legius syndrome

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

Pediatric Dermatology Consult - December 2016

Legius Syndrome - an overview

Part 1: Café-au-lait macule – Presentation and genesis

Legius Syndrome - an overview

Legius syndrome

Table 1 from SPRED 1 Mutations in a Neurofibromatosis Clinic

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

Noonan syndrome: improving recognition and diagnosis

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