Please use this identifier to cite or link to this item: https://doi.org/10.1097/TEN.0b013e3181693d5e
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dc.titlePhenotypic expression and challenges of a distinct form of thyrotoxicosis: Triiodothyronine-predominant Graves disease - Aggressive, refractory, and anything but banal
dc.contributor.authorDalan R.
dc.contributor.authorKon W.
dc.contributor.authorLeow M.K.S.
dc.date.accessioned2020-10-20T01:25:06Z
dc.date.available2020-10-20T01:25:06Z
dc.date.issued2008
dc.identifier.citationDalan R., Kon W., Leow M.K.S. (2008). Phenotypic expression and challenges of a distinct form of thyrotoxicosis: Triiodothyronine-predominant Graves disease - Aggressive, refractory, and anything but banal. Endocrinologist 18 (2) : 90 - 94. ScholarBank@NUS Repository. https://doi.org/10.1097/TEN.0b013e3181693d5e
dc.identifier.issn10512144
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/177746
dc.description.abstractTriiodothyronine (T3)-predominant Graves disease is characterized by persistently high serum T3 level and normal or low serum thyroxine (T4) level during thionamide drug therapy. Graves disease is much more aggressive in this form and has a lower remission rate with antithyroid drugs (ADI) and radioiodine (I-131) therapy. An 18-year-old Chinese woman had thyrotoxicosis with overt features of T3-predominant Graves disease. She failed to achieve a remission despite ADI treatment for 4 years and 3 doses of I-131 therapy. She finally underwent a total thyroidectomy followed by I-131 remnant ablation. The pathogenetic mechanisms, and the reasons for a tendency for nonremission with ADI, and I-131 therapy are discussed. 2008 Lippincott Williams & Wilkins, Inc.
dc.publisherLippincott Williams & Wilkins, Inc.
dc.sourceScopus
dc.subjectGraves' disease
dc.subjectT3-predominant thyrotoxicosis
dc.subjectThyroxine
dc.subjectTriiodothyronine
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1097/TEN.0b013e3181693d5e
dc.description.sourcetitleEndocrinologist
dc.description.volume18
dc.description.issue2
dc.description.page90 - 94
dc.published.statePublished
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