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Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects

Alport Syndrome is a genetic disorder characterized by hematuria, which often leads to renal failure. It may also be accompanied by extra-renal alterations, such as: sensorineural hearing loss, and ocular abnormalities. Dominant forms related to the X chromosome and caused by mutations in the locus...

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Detalles Bibliográficos
Autores principales: Alves, Fátima R.A., Quintanilha Ribeiro, Fernando de A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443539/
https://www.ncbi.nlm.nih.gov/pubmed/16878253
http://dx.doi.org/10.1016/S1808-8694(15)31253-2