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Uveitis and Multiple Sclerosis: Potential Common Causal Mutations

Uveitis, defined as inflammation of the uveal tract of the eye, is a leading cause of blindness and visual impairment throughout the world. The etiology of uveitis is complex, and autoimmunity plays a major role in its pathogenesis. Intermediate uveitis (IU), a subtype of ocular inflammation, has be...

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Detalles Bibliográficos
Autores Principales: de-la-Torre, Alejandra, Silva-Aldana, Claudia T., Muñoz-Ortiz, Juliana, Piñeros-Hernández, Laura B., Otero, Oscar, Domínguez, Alejandra, Faciolince, León A., Arcos-Holzinger, Mauricio, Mastronardi, Claudio, Contreras-Bravo, Nora Constanza, Restrepo, Carlos M., Arcos-Burgos, Mauricio
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: Humana Press Inc. 2019
Materias:
B cell activating factor
Adolescent
Adult
Article
BAFF gene
Child
Comorbidity
Controlled study
CPAMD8 gene
DGKI gene
Disease association
Female
Gene
Gene expression
Gene mutation
Gene segregation
Genetic analysis
Genetic linkage
GNGT1 gene
Heterozygosity
Homozygosity
Human
Intermediate uveitis
Male
Minimal critical region
Multiple sclerosis
Pathogenesis
School child
TNFRSF10A gene
Whole exome sequencing
Young adult
Complication
Diagnostic imaging
Genetics
Mutation
Pedigree
Procedures
Uveitis
Humans
Multiple Sclerosis
Whole Exome Sequencing
Young Adult
Mutations
Acceso en línea:https://repository.urosario.edu.co/handle/10336/22619
https://doi.org/10.1007/s12035-019-1630-2

Internet

https://repository.urosario.edu.co/handle/10336/22619
https://doi.org/10.1007/s12035-019-1630-2

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