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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...
Autores principales: | Alves, Fátima R.A., Quintanilha Ribeiro, Fernando de A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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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 |
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