[A Case of Pseudohypoaldosteronism Type â¡ (PHA2) Caused by a Novel Mutation of <i>KLHL</i>3].

Tang, Wei-Wei; Ma, Wan-Xia; Sun, Shi-Yi; Ran, Xing-Wu

[A Case of Pseudohypoaldosteronism Type â¡ (PHA2) Caused by a Novel Mutation of KLHL3].

Tang, Wei-Wei; Ma, Wan-Xia; Sun, Shi-Yi; Ran, Xing-Wu.

Afiliação

Tang WW; Diabetic Foot Care Centre, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu 610041, China.
Ma WX; Diabetic Foot Care Centre, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu 610041, China.
Sun SY; Diabetic Foot Care Centre, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu 610041, China.
Ran XW; Diabetic Foot Care Centre, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu 610041, China.

Sichuan Da Xue Xue Bao Yi Xue Ban ; 52(5): 890-894, 2021 Sep.

Article em Zh | MEDLINE | ID: mdl-34622611

Assuntos

Hipertensão; Pseudo-Hipoaldosteronismo; Proteínas Adaptadoras de Transdução de Sinal; Adulto; Aldosterona; Feminino; Humanos; Proteínas dos Microfilamentos; Mutação; Potássio; Pseudo-Hipoaldosteronismo/diagnóstico; Pseudo-Hipoaldosteronismo/genética

Palavras-chave

Gene mutation; Gordon syndrome; Hydrochlorothiazide hydrochloride; Hyperkalemia; Metabolic acidosis; Pseudohypoaldosteronism type â¡; Single gene inheritance disease

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pseudo-Hipoaldosteronismo / Hipertensão Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article

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