Legius Syndrome - an overview
Por um escritor misterioso
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Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2018;23:294-297]
Neurofibromatosis Type 1: Practice Essentials, Background, Pathophysiology
Legius syndrome: case report and review of literature – ScienceOpen
Lisch nodules and iris mammillations in two siblings with familial legius syndrome - Bixel - 2020 - Clinical Case Reports - Wiley Online Library
Chinese patient with neurofibromatosis-Noonan syndrome caused by novel heterozygous NF1 exons 1–58 deletion: a case report, BMC Pediatrics
Inherited Condition with Many Birthmarks”, Legius Syndrome
An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots, Freckling, and Neurofibromas. An Update. Part I. Dermatological Clinical Criteria Diagnostic of the Disease
New research may help differentiate similar diagnoses - Levenson - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Café-au-lait macule differential by craniofacial examination. Many of
