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Coexistence of Graves' Disease in a 14-year-old young girl with Gitelman Syndrome.

作者信息

Zha Bingbing, Zheng Pengxi, Liu Jun, Huang Xinmei

机构信息

Department of Endocrinology, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China.

出版信息

Clin Endocrinol (Oxf). 2015 Dec;83(6):995-7. doi: 10.1111/cen.12800. Epub 2015 May 7.

DOI:10.1111/cen.12800
PMID:25892104
Abstract
摘要

相似文献

1
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Puzzles in practice. Case report. A 62-year-old black woman with known Graves' disease. Diagnosis: Graves' dermopathy (elephantiasic type) and Graves' acropachy.实践中的难题。病例报告。一名62岁患有已知格雷夫斯病的黑人女性。诊断:格雷夫斯皮肤病(象皮病型)和格雷夫斯杵状指。
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A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature.一个新的 SLC12A3 基因突变导致 Gitelman 综合征合并自身免疫性甲状腺炎:病例报告及文献复习。
CEN Case Rep. 2024 Oct;13(5):330-338. doi: 10.1007/s13730-023-00845-z. Epub 2024 Feb 3.
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BMC Nephrol. 2023 May 2;24(1):123. doi: 10.1186/s12882-023-03180-8.
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Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous Mutations.两例 Gitelman 综合征家系合并蛋白尿或桥本甲状腺炎的临床分析及复合杂合突变研究
Biomed Res Int. 2021 May 10;2021:9973161. doi: 10.1155/2021/9973161. eCollection 2021.
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Genetic Analysis of SLC12A3 Gene in Chinese Patients with Gitelman Syndrome.SLC12A3 基因在中国 Gitelman 综合征患者中的遗传分析。
Med Sci Monit. 2019 Aug 9;25:5942-5952. doi: 10.12659/MSM.916069.
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Hypokalemia, hypomagnesemia, hypocalciuria, and recurrent tetany: Gitelman syndrome in a Chinese pedigree and literature review.低钾血症、低镁血症、低钙尿症及反复手足搐搦:一个中国家系中的吉特林综合征及文献复习
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