Ribeiro Magalhaes, Patricia KuenzleDare, Gustavo Leopoldo Rodriguesdos Santos, Sandra RodriguesNogueira, Célia Regina [UNESP]de Castro, MargaretMaciel, Lea Maria Zanini2014-05-202014-05-202007-11-01Clinical Endocrinology. Oxford: Blackwell Publishing, v. 67, n. 5, p. 748-753, 2007.0300-0664http://hdl.handle.net/11449/36337Objective Resistance to thyroid hormone (RTH) is a dominantly inherited syndrome of reduced tissue responsiveness to thyroid hormone usually due to mutations located in the ligand-binding domain and adjacent hinge region of the thyroid hormone receptor beta (TR beta). In the present report we describe the clinical and laboratory characteristics and the genetic analysis of patients with this rare disorder from a Brazilian population.Patients Four unrelated Brazilian families with diagnosis of RTH were studied. Age at diagnosis varied from 14 months to 29 years.Results All affected individuals were clinically euthyroid, except for one patient who presented immediately after birth with hyperthyroidism. All individuals had tachycardia and goitre, elevated concentrations of free thyroid hormones and reduced sensitivity to thyroid hormone. Direct sequencing analysis of the TR beta gene revealed four previously reported mutations: c.949G -> A, c.1313G -> A, c.1357C -> A and c.1358dupC in families A, B, C and D, respectively.Conclusion the present report shows that the frequent mutations described in the thyroid hormone receptor worldwide are also present in the Brazilian population, which is characterized by a variable ethnic background.748-753engArtigo10.1111/j.1365-2265.2007.02956.xWOS:000250253000018Acesso restrito