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REFERENCES
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- Devriendt K, Vanhole C, Matthijs G, de Zegher F. Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure. N Engl J Med 1998;338:1317-1318.
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thyroid dysgenesis-still an enigma after all these years. J Clin
Endocrinol Metab 2002;87:4069-4071.
- American Academy of Pediatrics AAP Section on Endocrinology and Committee on Genetics, and American Thyroid Association Committee on Public Health: Newborn screening for congenital hypothyroidism: recommended guidelines. Pediatrics 1993;91:1203-1209.
- Bongers-Schokking JJ, Koot HM, Wiersma D, Verkerk PH, de Muinck Keizer-Schrama SM. Influence of timing and dose of thyroid hormone replacement on development in infants with congenital hypothyroidism. J
Pediatr. 2000;136:292-297.
- Fisher DA, Foley BL. Early treatment of congenital hypothyroidism. Pediatrics. 1989;83:785-789.
- Brown RS, Bellisario RL, Botero D, et al. Incidence of transient congenital hypothyroidism due to maternal thyrotropin receptor-blocking antibodies in over one million babies. J Clin Endocrinol Metab 1996;81:1147-1151.
- Matsuura N, Konishi J, Transient hypothyroidism in infants born to mothers with chronic thyroiditis–a nationwide study of twenty-three cases. Endocrinol Jpn. 1990;37:369-379.
- Brown RS, Keating P, Mitchell E. Maternal thyroid-blocking immunoglobulins in congenital hypothyroidism. J Clin Endocrinol
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