Alström Syndrome: Genetics and Clinical Overview

Alström syndrome is a rare autosomal recessive genetic disorder characterized by cone-rod dystrophy, hearing loss, childhood truncal obesity, insulin resistance and hyperinsulinemia, type 2 diabetes, hypertriglyceridemia, short stature in adulthood, cardiomyopathy, and progressive pulmonary, hepatic...

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Detalles Bibliográficos
Autores principales: Marshall, Jan D, Maffei, Pietro, Collin, Gayle B, Naggert, Jürgen K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137007/
https://www.ncbi.nlm.nih.gov/pubmed/22043170
http://dx.doi.org/10.2174/138920211795677912

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137007/
https://www.ncbi.nlm.nih.gov/pubmed/22043170
http://dx.doi.org/10.2174/138920211795677912

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