Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic

BACKGROUND: Heterozygous mutations in the HNF1B gene are the most common monogenic cause of developmental kidney disease. Extrarenal phenotypes frequently occur, including diabetes mellitus and pancreatic hypoplasia; the latter is associated with subclinical exocrine dysfunction. We measured faecal...

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Detalles Bibliográficos
Autores principales: Clissold, Rhian L, Fulford, Jon, Hudson, Michelle, Shields, Beverley M, McDonald, Timothy J, Ellard, Sian, Hattersley, Andrew T, Bingham, Coralie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Genetic Kidney Diseases
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070112/
https://www.ncbi.nlm.nih.gov/pubmed/30094008
http://dx.doi.org/10.1093/ckj/sfx150

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070112/
https://www.ncbi.nlm.nih.gov/pubmed/30094008
http://dx.doi.org/10.1093/ckj/sfx150

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