Legius Syndrome
Dec. 23, 2024
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype | Journal of Medical Genetics Multiple café-au-lait maculae on the back of a child with Legius syndrome | Download Scientific Diagram 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 Legius Syndrome
![Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2018;23:294-297]](https://www.hkjpaed.org/figure/2018;23;294-297-fig1.jpg){kind=link}
![PDF] Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome. | …](https://d3i71xaburhd42.cloudfront.net/0fd4f69c196828ff2c10d42372299c717092c56b/4-Figure2-1.png){kind=link}
![PDF] Legius Syndrome, an Update.Molecular Pathology of Mutations in SPRED1 by undef…](https://og.oa.mg/Legius%20Syndrome%2C%20an%20Update.Molecular%20Pathology%20of%20Mutations%20in%20SPRED1.png?author=%20undefined,%20undefined){kind=link}
![PDF] Legius syndrome, an Update. Molecular pathology of mutations in SPRED1. | Sema…](https://d3i71xaburhd42.cloudfront.net/740cbef79c6b1777bfe82ab4e21b28448d7c04af/3-Table1-1.png){kind=link}
