Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease

Mutations in hepatocyte nuclear factor 1β gene (HNF1B) are responsible for a multisystemic syndrome where monogenic diabetes (classically known as MODY 5) and renal anomalies, mostly cysts, are the most characteristic findings. Urogenital malformations, altered liver function tests, hypomagnesemia o...

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Detalles Bibliográficos
Autores principales: Carrillo, Elena, Lomas, Amparo, Pinés, Pedro J, Lamas, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2017
Materias:
Insight into Disease Pathogenesis or Mechanism of Therapy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488326/
https://www.ncbi.nlm.nih.gov/pubmed/28680642
http://dx.doi.org/10.1530/EDM-17-0052

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488326/
https://www.ncbi.nlm.nih.gov/pubmed/28680642
http://dx.doi.org/10.1530/EDM-17-0052

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