Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects

Kanako Tanase‐Nakao; Megumi Iwahashi-Odano; Chiho Sugisawa; Kiyomi Abe; Koji Muroya; Yukiyo Yamamoto; Yasusada Kawada; Yuichi Mushimoto; Kazuhiro Ohkubo; Saori Kinjo; Kazuhiro Shimura; Kohei Aoyama; Haruo Mizuno; Tomoyuki Hotsubo; Chie Takahashi; Tsuyoshi Isojima; Yoko Kina; Satoshi Takakuwa; Junpei Hamada; Miwa Sawaki; Keiichi Shigehara; Satoru Sugimoto; Yuri Etani; Hiroko Narumi-Wakayama; Yusuke Mine; Tomonobu Hasegawa; Akira Hishinuma; Satoshi Narumi

doi:10.1210/clinem/dgae098

Abstract

Thyroglobulin (Tg), encoded by TG, is essential for thyroid hormone synthesis. TG defects result in congenital hypothyroidism (CH). Most reported patients were born before the introduction of newborn screening (NBS).

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Tanase‐Nakao et al. (2024) studied this question.

synapsesocial.com/papers/68e78950b6db6435876fb847 https://doi.org/10.1210/clinem/dgae098

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Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects

Abstract

Discussion

Cite This Study

Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects

Abstract

Discussion

Cite This Study

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