Nephrogenic syndrome of inappropriate antidiuresis - An ethnically, genetically and phenotypically diverse disorder: First report in a Chinese adult and review of published cases.

Tong, Hok Fung; Leung, Mei Tik Stella; Chan, Chun Hei Toby; Cheung, Hoi Ning; Mak, Wing Lai Tony; Chen, Pak Lam Sammy

Tong, Hok Fung; Leung, Mei Tik Stella; Chan, Chun Hei Toby; Cheung, Hoi Ning; Mak, Wing Lai Tony; Chen, Pak Lam Sammy.

Afiliação

Tong HF; Department of Pathology, Princess Margaret Hospital, Hong Kong. Electronic address: thf141@ha.org.hk.
Leung MTS; Department of Pathology, Queen Elizabeth Hospital, Hong Kong.
Chan CHT; Department of Pathology, Queen Elizabeth Hospital, Hong Kong; Department of Pathology, Hong Kong Children's Hospital, Hong Kong.
Cheung HN; Department of Pathology, Queen Elizabeth Hospital, Hong Kong.
Mak WLT; Department of Pathology, Princess Margaret Hospital, Hong Kong.
Chen PLS; Department of Pathology, Queen Elizabeth Hospital, Hong Kong.

Clin Chim Acta ; 519: 214-219, 2021 Aug.

Article em En | MEDLINE | ID: mdl-33984325

Assuntos

Diabetes Insípido Nefrogênico; Doenças Genéticas Ligadas ao Cromossomo X; Síndrome de Secreção Inadequada de HAD; Adulto; China; Humanos; Síndrome de Secreção Inadequada de HAD/diagnóstico; Síndrome de Secreção Inadequada de HAD/genética; Masculino; Receptores de Vasopressinas/genética

Palavras-chave

AVPR2; Gsα; Hyponatraemia; Nephrogenic syndrome of inappropriate antidiuresis; V2R

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Insípido Nefrogênico / Doenças Genéticas Ligadas ao Cromossomo X / Síndrome de Secreção Inadequada de HAD Tipo de estudo: Diagnostic_studies Limite: Adult / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Clin Chim Acta Ano de publicação: 2021 Tipo de documento: Article

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