1 From the Department of Pediatrics, University of California, Davis, School of Medicine, Davis
Recognition of transient forms of neonatal hypothyroidism is difficult because of the urgency of thyroxine treatment. In the present report the first child born to a mother with Graves' disease developed transient hyperthyroidism during the newborn period. The mother underwent radioactive iodine treatment and was maintained euthyroid on l-thyroxine. Two subsequent children were detected by newborn thyroid screen to have low thyroxine and markedly elevated serum thyrotropin (TSH) levels. Technetium 99 metastable and iodine 123 scans at 22 days of age showed the second child to be athyreotic. The third child was not scanned. All three children were nongoitrous at birth. Patients 2 and 3 had continuous TSH suppression with thyroxine therapy for 3 and 4 years. Thyroid function measurements after discontinuation of therapy for 8 weeks were normal, and both children had normal 123I thyroid scans. The mother was found to have potent TSH-binding inhibitory immunoglobulin (TBII) levels in her serum (85.5%). A fourth child with low thyroxine and elevated TSH was born to a mother on a regimen of l-thyroxine for hypothyroidism. 99mTc scan at 26 days of age showed no thyroid tissue and was normal at 3 months. TBII activity was 35% in the maternal serum and absent in the infant's serum. The above laboratory and clinical data are compatible with the blocking nature of TBII, resulting in transient newborn hypothyroidism and an athyreotic appearance on scan. The TBII measurement can be a useful predictor of neonatal hypothyroidism as well as confirm the transient nature of the disease in newborns.
Key Words: transient congenital hypothyroidism thyrotropin-binding inhibitory immunoglobulin maternal thyroid antibody
Accepted on December 16, 1985
This article has been cited by other articles:
![]() |
J. Cleary-Goldman, F. D. Malone, G. Lambert-Messerlian, L. Sullivan, J. Canick, T. F. Porter, D. Luthy, S. Gross, D. W. Bianchi, M. E. D'Alton, et al. Maternal Thyroid Hypofunction and Pregnancy Outcome Obstet. Gynecol., July 1, 2008; 112(1): 85 - 92. [Abstract] [Full Text] [PDF] |
||||
![]() |
A L Ogilvy-Stuart Neonatal thyroid disorders Arch. Dis. Child. Fetal Neonatal Ed., November 1, 2002; 87(3): F165 - 171. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Haddow, G. E. Palomaki, W. C. Allan, J. R. Williams, G. J. Knight, J. Gagnon, C. E. O'Heir, M. L. Mitchell, R. J. Hermos, S. E. Waisbren, et al. Maternal Thyroid Deficiency during Pregnancy and Subsequent Neuropsychological Development of the Child N. Engl. J. Med., August 19, 1999; 341(8): 549 - 555. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Devos, C. Rodd, N. Gagné, R. Laframboise, and G. Van Vliet A Search for the Possible Molecular Mechanisms of Thyroid Dysgenesis: Sex Ratios and Associated Malformations J. Clin. Endocrinol. Metab., July 1, 1999; 84(7): 2502 - 2506. [Abstract] [Full Text] |
||||
![]() |
N. Gagné, J. Parma, C. Deal, G. Vassart, and G. Van Vliet Apparent Congenital Athyreosis Contrasting with Normal Plasma Thyroglobulin Levels and Associated with Inactivating Mutations in the Thyrotropin Receptor Gene: Are Athyreosis and Ectopic Thyroid Distinct Entities? J. Clin. Endocrinol. Metab., May 1, 1998; 83(5): 1771 - 1775. [Abstract] [Full Text] |
||||
![]() |
L. D. Kohn, K. Suzuki, W. H. Hoffman, D. Tombaccini, C. Marcocci, N. Shimojo, Y. Watanabe, N. Amino, B. Y. Cho, Y. Kohno, et al. Characterization of Monoclonal Thyroid-Stimulating and Thyrotropin Binding-Inhibiting Autoantibodies from a Hashimoto's Patient Whose Children Had Intrauterine and Neonatal Thyroid Disease J. Clin. Endocrinol. Metab., December 1, 1997; 82(12): 3998 - 4009. [Abstract] [Full Text] [PDF] |
||||