Cargando…
Legius Syndrome and its Relationship with Neurofibromatosis Type 1
Neurofibromatosis type 1 (NF1) is the most common disorder characterized by multiple café-au-lait macules. Most individuals with this autosomal dominant disorder also have other features, such as skinfold freckling, iris Lisch nodules and benign or malignant peripheral nerve sheath tumours. Legius s...
Autores principales: | DENAYER, Ellen, LEGIUS, Eric |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Publication of Acta Dermato-Venereologica
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9128993/ https://www.ncbi.nlm.nih.gov/pubmed/32147744 http://dx.doi.org/10.2340/00015555-3429 |
Ejemplares similares
-
Legius Syndrome in Fourteen Families
por: Denayer, Ellen, et al.
Publicado: (2011) -
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation
por: Legius, Eric, et al.
Publicado: (2021) -
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders
por: Giugliano, Teresa, et al.
Publicado: (2019) -
Understanding the Interactions between the Proteins Implicated in Legius Syndrome and Neurofibromatosis Type 1(♦): Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1
Publicado: (2016) -
The SPRED1 Variants Repository for Legius Syndrome
por: Sumner, Kelli, et al.
Publicado: (2011)