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Acquired Bartter Syndrome in Primary Sjögren Syndrome
Author(s) -
A. Fraj,
M. El Euch,
F. Jaziri,
A. Kefi,
K. Ben Abdelghani,
S. Turki,
T. Ben Abdallah
Publication year - 2020
Publication title -
saudi journal of kidney diseases and transplantation/našrat amraḍ wa zira'aẗ al-kulaẗ
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.268
H-Index - 30
eISSN - 2320-3838
pISSN - 1319-2442
DOI - 10.4103/1319-2442.301185
Subject(s) - medicine , bartter syndrome , nephrogenic diabetes insipidus , renal tubular acidosis , distal renal tubular acidosis , fanconi syndrome , dermatology , tubulopathy , diabetes insipidus , endocrinology , gastroenterology , pediatrics , kidney , hypokalemia , acidosis
Renal tubular involvement in Sjögren's syndrome (SS) often described with renal tubular acidosis, nephrogenic diabetes insipidus, or rarely with Fanconi syndrome. SS presenting with clinical features of Bartter's syndrome or Gitelman's syndrome is rare. We report a case of a female patient who presented an acquired Bartter syndrome with a primary SS.

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