2007Kidney Research and Clinical PracticeOpen access

A case of Gitelman's Syndrome with Chronic Hypotension and Normomagnesemia

Hae-Jung Jun, Su-Kyung Cho, Sang-Bun Choi, Jeong-Sook Seo, Sun-Woo Kang, Yeung-Hoon Kim, Miseon Kang, Wan‐Young Kim, Jin Kim, Yang-Wook Kim

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Abstract

Gitelman's syndrome is a heritable renal disorder characterized by hypomagnesemia, hypokalemia and hypocalciuria. Interestingly, we have experienced one patient who had chronic hypotension, normal serum magnesium level, normal plasma ionized magnesium level, hypokalemia and hypocalciuria. Immunohistochemistry showed the absence of NCCT staining in renal tissues of the patient. We report the case of atypical Gitelman's syndrome with a brief review of related literature.

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What this paper is about

Gitelman's syndrome is a heritable renal disorder characterized by hypomagnesemia, hypokalemia and hypocalciuria. Interestingly, we have experienced one patient who had chronic hypotension, normal serum magnesium level, normal plasma ionized magnesium level, hypokalemia and hypocalciuria. Immunohistochemistry showed the absence of NCCT staining in renal tissues of the patient. We report the case of atypical Gitelman's syndrome with a brief review of related literature.

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Available abstract

Gitelman's syndrome is a heritable renal disorder characterized by hypomagnesemia, hypokalemia and hypocalciuria. Interestingly, we have experienced one patient who had chronic hypotension, normal serum magnesium level, normal plasma ionized magnesium level, hypokalemia and hypocalciuria. Immunohistochemistry showed the absence of NCCT staining in renal tissues of the patient. We report the case of atypical Gitelman's syndrome with a brief review of related literature.

Key concepts: Hypocalciuria, Hypomagnesemia, Medicine, Hypokalemia, Gitelman syndrome, Internal medicine, Gastroenterology, Magnesium

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