A case report of pseudohypoaldosteronism type II with a homozygous KLHL3 variant accompanied by hyperthyroidism

A case report of pseudohypoaldosteronism type II with a homozygous KLHL3 variant accompanied by hyperthyroidism

Abstract Background Pseudohypoaldosteronism type II (PHAII), also called Gordon syndrome, is a rare hereditary disease caused by variants in the WNK1, WNK4, KLHL3 and CUL3 genes. The combination of PHAII with hyperthyroidism and secondary hyperparathyroidism has not been reported previously. Case pr...

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Bibliographic Details
Main Authors: Rui Zhang, Simin Zhang, Yingying Luo, Meng Li, Xin Wen, Xiaoling Cai, Xueyao Han, Linong Ji
Format: Article
Language:English
Published: BMC 2021-05-01
Series:BMC Endocrine Disorders
Subjects:
Pseudohypoaldosteronism type II
Hyperkalemia
Secondary hyperparathyroidism
Hyperthyroidism
Case report
Online Access:https://doi.org/10.1186/s12902-021-00767-w

Internet

https://doi.org/10.1186/s12902-021-00767-w

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