A 7-year-old girl presenting with a Bartter-like phenotype: Questions

Pediatr Nephrol. 2017 Jun;32(6):981-982. doi: 10.1007/s00467-016-3473-7. Epub 2016 Aug 17.

Yunsoo Choe¹, Eujin Park¹, Hye Sun Hyun¹, Jung Min Ko^{1

2}, Hee Gyung Kang^{1

2}, Jeong Hun Kim³, Sung-Hye Park⁴, Hae Il Cheong^{5

6

7}

¹ Department of Pediatrics, Seoul National University Children's Hospital, 101 Daehak-Ro, Jongno-Gu, Seoul, 03080, Korea.
² Research Coordination Center for Rare Diseases, Seoul National University Hospital, Seoul, Korea.
³ Department of Biomedical Sciences, Clinical Sciences, and Ophthalmology, Seoul National University College of Medicine, Seoul, Korea.
⁴ Department of Pathology, Seoul National University College of Medicine, Seoul, Korea.
⁵ Department of Pediatrics, Seoul National University Children's Hospital, 101 Daehak-Ro, Jongno-Gu, Seoul, 03080, Korea. [email protected].
⁶ Research Coordination Center for Rare Diseases, Seoul National University Hospital, Seoul, Korea. [email protected].
⁷ Kidney Research Institute, Medical Research Center, Seoul National University College of Medicine, Seoul, Korea. [email protected].

No abstract available

Keywords: Bartter-like phenotype; Failure to thrive; Hypoparathyroidism; Muscle weakness; Proximal renal tubulopathy; Sensorineural hearing loss.

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