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Thyrotropin Secretion in Thalassemic Patients during Puberty and Postpuberty

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Frontiers in Thyroidology

Abstract

Hypogonadotropic hypogonadism attributed to hemosiderosis is frequent in patients with beta-thalassemia major (1,2). Data concerning the other pituitary and peripheral endocrine hormones are controversial. In a previous study (3), we found low thyroid hormone concentrations and/or increased serum TSH levels in a high percentage of clinically euthyroid patients. This situation was found in early childhood and did not change with increasing age. Compensated hypothyroidism with high or normal TSH levels which were hyperresponsive to TRH was described by several authors (4–6) in thalassemic patients, whereas others report normal indices of thyroid function (1,7).

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© 1986 Springer Science+Business Media New York

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Langer, M. et al. (1986). Thyrotropin Secretion in Thalassemic Patients during Puberty and Postpuberty. In: Medeiros-Neto, G., Gaitan, E. (eds) Frontiers in Thyroidology. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5260-0_44

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  • DOI: https://doi.org/10.1007/978-1-4684-5260-0_44

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-5262-4

  • Online ISBN: 978-1-4684-5260-0

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