A Case of Gitelman Syndrome that Was Difficult to Distinguish from Hypokalemic Periodic Paralysis Caused by Graves' Disease-Reference-Cited by-同舟云学术

A Case of Gitelman Syndrome that Was Difficult to Distinguish from Hypokalemic Periodic Paralysis Caused by Graves' Disease

Published:2019-10-15 Issue:5 Volume:86 Page:301-306
ISSN:1345-4676
Container-title:Journal of Nippon Medical School
language:en
Short-container-title:J Nippon Med Sch

Author:

Oba Takeshi¹,Kobayashi Shunsuke¹,Nakamura Yuko¹,Nagao Mototsugu¹,Nozu Kandai²,Fukuda Izumi¹,Iijima Kazumoto²,Sugihara Hitoshi¹

Affiliation:

1. Department of Endocrinology, Diabetes and Metabolism, Graduate School of Medicine, Nippon Medical School

2. Department of Pediatrics, Kobe University Graduate School of Medicine

Publisher

Medical Association of Nippon Medical School

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/jnms/86/5/86_JNMS.2019_86-505/_pdf

Reference26 articles.

1. 1. Abbasi B, Sharif Z, Sprabery LR: Hypokalemic thyrotoxic periodic paralysis with thyrotoxic psychosis and hypercapnic respiratory failure. Am J Med Sci 2010; 340: 147-153.

2. 2. Pothiwala P, Levine SN: Analytic review: thyrotoxic periodic paralysis: a review. J Intensive Care Med 2010; 25: 71-77.

3. 3. Gitelman HJ, Graham JB, Welt LG: A new familial disorder characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians 1966; 79: 92-96.

4. 4. Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M: The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies. J Clin Endocrinol Metab 2010; 95: 511-518.

5. 5. Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP: Gilelman's variant of Batter's syndrome, inherited hypokalemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat Genet 1996; 12: 24-30.

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