A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter’s syndrome with 4 years follow-up

A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter’s syndrome with 4 years follow-up

Abstract Background Transient antenatal Bartter’s syndrome caused by MAGED2 mutation is a rare X-linked recessive renal tubular disorder. Cases reported are mostly infants, and the long-term prognosis of the disease is still under investigation. Case presentation We encountered a preterm male infant...

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Bibliographic Details
Main Authors: Mingsheng Ma, Mengqi Zhang, Yu Zhou, Fengxia Yao, Min Wei, Zhenghong Li, Zhengqing Qiu
Format: Article
Language:English
Published: BMC 2021-12-01
Series:BMC Nephrology
Subjects:
MAGED2 gene
Transient antenatal Bartter’s syndrome
Polyhydramnios
Case report
Online Access:https://doi.org/10.1186/s12882-021-02553-1

Internet

https://doi.org/10.1186/s12882-021-02553-1

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