Case Reports of Familial Non-autoimmune Hyperthyroidism in Two Malaysian Families due to Germline-activating Mutations in the Thyrotropin Receptor Gene
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This article is published under the Creative Commons Attribution Non-commercial License.
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Touch Medical Media, Ltd.
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Endocrinology, Diabetes and Metabolism
Reference20 articles.
1. Bahn RS, Burch HB, Cooper DS, et al. Hyperthyroidism and other causes of thyrotoxicosis: management guidelines of the American Thyroid Association and American Association of Clinical Endocrinologists. Endocr Pract. 2011;17:456–520.
2. Forssberg M, Arvidsson CG, Engvall J, et al. Increasing incidence of childhood thyrotoxicosis in a population-based area of central Sweden. Acta Paediatr. 2004;93:25–9.
3. Thomas JL, Leclere J, Hartemann P, et al. Familial hyperthyroidism without evidence of autoimmunity. Acta Endocrinol-Cop. 1982;100:512–8.
4. Duprez L, Parma J, Vansande J, et al. Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal-dominant hyperthyroidism. Nat Genet. 1994;7:396–401.
5. Pohlenz J, Pfarr N, Kruger S, Hesse V. Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R). Acta Paediatrica. 2006;95:1685–7.
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