Clinical and genetic characteristics of 29 Chinese patients with X-linked hypophosphatemia.

Xu, Tian; Tao, Xiaohui; Zhang, Zhenlin; Yue, Hua

Xu, Tian; Tao, Xiaohui; Zhang, Zhenlin; Yue, Hua.

Afiliação

Xu T; Shanghai Clinical Research Center of Bone Diseases, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Tao X; Shanghai Clinical Research Center of Bone Diseases, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Zhang Z; Shanghai Clinical Research Center of Bone Diseases, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Yue H; Shanghai Clinical Research Center of Bone Diseases, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

Front Endocrinol (Lausanne) ; 13: 956646, 2022.

Article em En | MEDLINE | ID: mdl-36060934

Assuntos

Raquitismo Hipofosfatêmico Familiar; Hipofosfatemia; China/epidemiologia; Raquitismo Hipofosfatêmico Familiar/genética; Feminino; Humanos; Masculino; Endopeptidase Neutra Reguladora de Fosfato PHEX/genética; Maturidade Sexual

Palavras-chave

PHEX; X-linked dominant hypophosphatemia; clinical features; fibroblast growth factor 23; gene mutation

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipofosfatemia / Raquitismo Hipofosfatêmico Familiar Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Front Endocrinol (Lausanne) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Suíça

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