Usefulness of Early Genetic Diagnosis for Twins With a Family History of Congenital Nephrotic Syndrome.

Toya, Yukiko; Ishikawa, Ken; Yoshida, Taro; Matsumoto, Atsushi; Akasaka, Manami; Nozu, Kandai

Toya, Yukiko; Ishikawa, Ken; Yoshida, Taro; Matsumoto, Atsushi; Akasaka, Manami; Nozu, Kandai.

Afiliação

Toya Y; Department of Pediatrics, Iwate Medical University, Iwate, JPN.
Ishikawa K; Department of Pediatrics, Iwate Medical University, Iwate, JPN.
Yoshida T; Department of Pediatrics, Iwate Medical University, Iwate, JPN.
Matsumoto A; Department of Pediatrics, Iwate Medical University, Iwate, JPN.
Akasaka M; Department of Pediatrics, Iwate Medical University, Iwate, JPN.
Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, JPN.

Cureus ; 15(3): e36667, 2023 Mar.

Article em En | MEDLINE | ID: mdl-37101999

Palavras-chave

congenital anomaly; early diagnosis and treatment; finnish-type congenital nephrotic syndrome; genetic test; twin pregnancies

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: En Revista: Cureus Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos

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