Multiple neoplasia in a patient with Gitelman syndrome harboring germline monoallelic MUTYH mutation

Multiple neoplasia in a patient with Gitelman syndrome harboring germline monoallelic MUTYH mutation

Gitelman syndrome is a rare, recessively inherited disease characterized by chronic hypokalemia and hypomagnesemia as a result of defective electrolyte co-transport at the level of the distal convoluted tubule of the kidney. Here, we present the first report of a patient with Gitelman syndrome who d...

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Bibliographic Details
Main Authors: Chan, Jason Yongsheng, Toh, Ming Ren, Chong, Siao Ting, Nur Diana Ishak, Kolinjivadi, Arun Mouli, Chan, Sock Hoai, Lee, Elizabeth, Boot, Arnoud, Shao-Tzu, Li, Chew, Min-Hoe, Ngeow, Joanne
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2021
Subjects:
Science::Medicine
Cancer Genetics
Genetics Research
Online Access:https://hdl.handle.net/10356/146678
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Institution: Nanyang Technological University
Language: English

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https://hdl.handle.net/10356/146678

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