Knowns and unknowns about congenital hypothyroidism: 2022 update.

Itonaga, Tomoyo; Hasegawa, Yukihiro; Higuchi, Shinji; Satoh, Mari; Sawada, Hirotake; Shimura, Kazuhiro; Takahashi, Ikuko; Takubo, Noriyuki; Nagasaki, Keisuke

Itonaga, Tomoyo; Hasegawa, Yukihiro; Higuchi, Shinji; Satoh, Mari; Sawada, Hirotake; Shimura, Kazuhiro; Takahashi, Ikuko; Takubo, Noriyuki; Nagasaki, Keisuke.

Afiliación

Itonaga T; Department of Pediatrics, Oita University Faculty of Medicine, Oita, Japan.
Hasegawa Y; Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.
Higuchi S; Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.
Satoh M; Department of Pediatrics, Toho University Omori Medical Center, Tokyo, Japan.
Sawada H; Division of Pediatrics, Faculty of Medicine, University of Miyazaki Hospital, Miyazaki, Japan.
Shimura K; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Takahashi I; Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan.
Takubo N; Department of Pediatrics and Adolescent Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Nagasaki K; Department of Pediatrics, Niigata University Medical and Dental Hospital, Niigata, Japan.

Clin Pediatr Endocrinol ; 32(1): 11-25, 2023.

Article en En | MEDLINE | ID: mdl-36761498

Palabras clave

congenital hypothyroidism; iodine; levothyroxine; molecular genetics; the dual oxidase 2 (DUOX2)

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline / Qualitative_research Idioma: En Revista: Clin Pediatr Endocrinol Año: 2023 Tipo del documento: Article País de afiliación: Japón

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