Legius Syndrome - an overview
Por um escritor misterioso
Last updated 27 março 2025


Syndromes The RASopathies Network

Legius syndrome - Wikipedia

RASopathies: Dermatologists' viewpoints - Indian Journal of Dermatology, Venereology and Leprology

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

PDF] Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome.

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

Abbreviations: LS, Legius syndrome; M, male; F, female. Individuals

Cutaneous Expression of Familial Cancer Syndromes, HTML

Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

Novel association of neurofibromatosis type 1‐causing mutations in families with neurofibromatosis‐noonan syndrome - Ekvall - 2014 - American Journal of Medical Genetics Part A - Wiley Online Library

Frontiers Novel Splicing Variant in the PMM2 Gene in a Patient With PMM2-CDG Syndrome Presenting With Pericardial Effusion: A Case Report

New research may help differentiate similar diagnoses - Levenson - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
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