Research Paper | Medicine | India | Volume 9 Issue 3, March 2020
Case Report: A Rare Presentation of Quadriplegia as Gitelman Syndrome
Dr L S Patil, Dr Yudhishther Kuntal
Abstract: Gitelman syndrome is an autosomal recessive disorder caused by the mutation of SLC12A3 or CLCNKB which encodes renal Na – Cl co transporter channels it causes imbalance of potassium magnesium and calcium metabolism. Gitelman symptoms are similar to thiazide diuretic-abusers with salt wasting. Gitelman syndrome, the defect resides at the distal convoluted tubule and rare cause of quadriplegia
Keywords: gitelman, quadriplegia, potassium
Edition: Volume 9 Issue 3, March 2020,
Pages: 184 - 185
How to Cite this Article?
Dr L S Patil, Dr Yudhishther Kuntal, "Case Report: A Rare Presentation of Quadriplegia as Gitelman Syndrome", International Journal of Science and Research (IJSR), https://www.ijsr.net/get_abstract.php?paper_id=SR20221151345, Volume 9 Issue 3, March 2020, 184 - 185
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