Subclinical Nonautoimmune Hyperthyroidism in a Family Segregates with a Thyrotropin Receptor Mutation with Weakly Increased Constitutive Activity

BACKGROUND: Subclinical hyperthyroidism is usually associated with Graves' disease or toxic nodular goiter. Here we report a family with hereditary subclinical hyperthyroidism caused by a constitutively activating germline mutation of the thyrotropin receptor (TSHR) gene. METHODS: The proband w...

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Autors principals: Nishihara, Eijun, Chen, Chun-Rong, Higashiyama, Takuya, Mizutori-Sasai, Yumiko, Ito, Mitsuru, Kubota, Sumihisa, Amino, Nobuyuki, Miyauchi, Akira, Rapoport, Basil
Format: Artigo
Idioma:Inglês
Publicat: Mary Ann Liebert, Inc. 2010
Matèries:
Case Study
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2974847/
https://ncbi.nlm.nih.gov/pubmed/20929407
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/thy.2010.0261
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