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Clinical and genetic features of Kenny-Caffey syndrome type 2 with multiple electrolyte disturbances: A case report.

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第一作者： Ning,Yuan

第一单位： Department of Endocrinology, Nanchong Central Hospital, The Second Clinical College, North Sichuan Medical College, Nanchong 637000, Sichuan Province, China.

作者： Ning,Yuan ^[1] ; Lin,Lu ^[2] ; Xiao-Ping,Xing ^[3] ; Ou,Wang ^[3] ; Yue,Jiang ^[3] ; Ji,Wu ^[4] ; Ming-Hai,He ^[1] ; Xiao-Juan,Wang ^[1] ; Le-Wei,Cao ^[1]

作者单位： Department of Endocrinology, Nanchong Central Hospital, The Second Clinical College, North Sichuan Medical College, Nanchong 637000, Sichuan Province, China. ^[1] Department of Endocrinology, Key Laboratory of National health commission, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing 100730, China. lulin88@sina.com. ^[2] Department of Endocrinology, Key Laboratory of National health commission, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing 100730, China. ^[3] Department of Urology, Nanchong Central Hospital, The Second Clinical College, North Sichuan Medical College, Nanchong 637000, Sichuan Province, China. ^[4]

关键词 Case report FAM111A gene Hypocalcemia Hypomagnesemia Hypoparathyroidism Kenny-Caffey syndrome type 2

DOI 10.12998/wjcc.v11.i10.2290

PMID 37122511

发布时间 2023-05-02

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World journal of clinical cases

2023年11卷10期

2290-2300页

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World journal of clinical cases

2023年11卷10期

2290-2300页

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Clinical and genetic features of Kenny-Caffey syndrome type 2 with multiple electrolyte disturbances: A case report.

World journal of clinical cases

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World journal of clinical cases

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Clinical and genetic features of Kenny-Caffey syndrome type 2 with multiple electrolyte disturbances: A case report.

World journal of clinical cases

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World journal of clinical cases

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