Familial Alström syndrome: a rare cause of bilateral progressive hearing loss ,

INTRODUCTION: Alström Syndrome is a rare disease caused by mutations in ALMS1 gene. It is characterized by a progressive degeneration of sensory functions, resulting in visual and audiological impairment, as well as metabolic disturbances such as childhood obesity, hyperinsulinemia, and diabetes mel...

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Detalles Bibliográficos
Autores principales: Bahmad, Fayez, Costa, Carolina Sousa Alves, Teixeira, Marina Santos, de Barros Filho, Jairo, Viana, Lucas Moura, Marshall, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Original article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443977/
https://www.ncbi.nlm.nih.gov/pubmed/24830966
http://dx.doi.org/10.5935/1808-8694.20140023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443977/
https://www.ncbi.nlm.nih.gov/pubmed/24830966
http://dx.doi.org/10.5935/1808-8694.20140023

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