Antenatal Bartter syndrome resembling nephrogenic diabetes insipidus in a 5-year-old boy

J Formos Med Assoc. 2016 May;115(5):382-3. doi: 10.1016/j.jfma.2015.03.017. Epub 2015 Apr 29.

Authors

Gwo-Tsann Chuang¹, Shih-Hua Lin², Yong-Kwei Tsau¹, I-Jung Tsai³

Affiliations

¹ Department of Pediatrics, National Taiwan University Children Hospital, Taipei, Taiwan.
² Division of Nephrology, Department of Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
³ Department of Pediatrics, National Taiwan University Children Hospital, Taipei, Taiwan. Electronic address: ijtsai@ntu.edu.tw.

PMID: 25935500
DOI: 10.1016/j.jfma.2015.03.017

No abstract available

Publication types

Case Reports

MeSH terms

Bartter Syndrome / complications*
Bartter Syndrome / genetics*
Child, Preschool
Diabetes Insipidus, Nephrogenic / diagnosis*
Humans
Male
Mutation
Solute Carrier Family 12, Member 1 / genetics*
Ultrasonography

Substances

SLC12A1 protein, human
Solute Carrier Family 12, Member 1