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

Yuan, Ning; Lu, Lin; Xing, Xiao-Ping; Wang, Ou; Jiang, Yue; Wu, Ji; He, Ming-Hai; Wang, Xiao-Juan; Cao, Le-Wei

Yuan, Ning; Lu, Lin; Xing, Xiao-Ping; Wang, Ou; Jiang, Yue; Wu, Ji; He, Ming-Hai; Wang, Xiao-Juan; Cao, Le-Wei.

Afiliação

Yuan N; Department of Endocrinology, Nanchong Central Hospital, The Second Clinical College, North Sichuan Medical College, Nanchong 637000, Sichuan Province, China.
Lu L; 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.
Xing XP; 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.
Wang O; 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.
Jiang Y; 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.
Wu J; Department of Urology, Nanchong Central Hospital, The Second Clinical College, North Sichuan Medical College, Nanchong 637000, Sichuan Province, China.
He MH; Department of Endocrinology, Nanchong Central Hospital, The Second Clinical College, North Sichuan Medical College, Nanchong 637000, Sichuan Province, China.
Wang XJ; Department of Endocrinology, Nanchong Central Hospital, The Second Clinical College, North Sichuan Medical College, Nanchong 637000, Sichuan Province, China.
Cao LW; Department of Endocrinology, Nanchong Central Hospital, The Second Clinical College, North Sichuan Medical College, Nanchong 637000, Sichuan Province, China.

World J Clin Cases ; 11(10): 2290-2300, 2023 Apr 06.

Article em En | MEDLINE | ID: mdl-37122511

Palavras-chave

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

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: World J Clin Cases Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

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