Title:
Sheehan syndrome with Gitelman syndrome, tackling additive morbidity

dc.contributor.authorSukdev Manna
dc.contributor.authorSankha Shubhra Chakrabarti
dc.contributor.authorDeepak Kumar Gautam
dc.contributor.authorIndrajeet Singh Gambhir
dc.date.accessioned2026-02-07T09:08:36Z
dc.date.issued2019
dc.description.abstractSheehan syndrome (SS) is postpartum hypopituitarism resulting from pituitary gland necrosis caused by severe hypotension due to massive intra or post-partum hemorrhage. Defective NaCl transport in the distal convoluted tubule, due to mutations affecting the thiazide sensitive Na-Cl-cotransporter results in the autosomal recessive salt-losing renal tubulopathy, Gitelman syndrome (GS). These two have been rarely described together. We report the case of a middle-aged woman with both these conditions, resulting in management issues. Physicians encountering unexplained hypokalemia refractory to standard management must consider the possibility of renal tubular disorders. © 2019, Iranian Society of Nephrology. All rights reserved.
dc.identifier.issn17358582
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/34382
dc.publisherIranian Society of Nephrology
dc.subjectHypokalemia
dc.subjectHypopituitarism
dc.subjectSpironolactone
dc.subjectTubulopathy
dc.titleSheehan syndrome with Gitelman syndrome, tackling additive morbidity
dc.typePublication
dspace.entity.typeArticle

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