Hereditary renal glycosuria, diabetes and responses to SGLT2 inhibitor

AIMS: To present the clinical features of two rare cases with hereditary renal glycosuria and diabetes, explore their responses to sodium‐glucose cotransporter 2 (SGLT2) inhibitor, and summarize the reported solute carrier family 5 member 2 (SLC5A2) mutations and related phenotypes. METHODS: Two pat...

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Detalles Bibliográficos
Autores principales: Ren, Qian, Gong, Siqian, Han, Xuyao, Ji, Linong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060016/
https://www.ncbi.nlm.nih.gov/pubmed/35229480
http://dx.doi.org/10.1111/1753-0407.13254

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060016/
https://www.ncbi.nlm.nih.gov/pubmed/35229480
http://dx.doi.org/10.1111/1753-0407.13254

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