Abstract
Resistance to thyroid hormone (RTH) is a rare syndrome of reduced responsiveness of target tissues to thyroid hormone and is caused mutation in the thyroid β receptor gene. We report a novel mutation, E445X, causing RTH in a 4-year old girl. The patient exhibited extreme signs and symptoms of RTH at an early age, and had a large compressive goiter. Following total extracapsular thyroidectomy, upper airway compression was relieved and symptoms of hyperthyroidism improved. This case appears to be the youngest child recorded to have undergone total thyroidectomy for RTH. Post-operative TSH elevations were managed with every-other-day triiodothyronine therapy.
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CITATION STYLE
Canadas, K. T., Rivkees, S. A., Udelsman, R., & Breuer, C. K. (2011). Resistance to thyroid hormone associated with a novel mutation of the thyroid β receptor gene in a four-year-old female. International Journal of Pediatric Endocrinology, 2011(1). https://doi.org/10.1186/1687-9856-2011-3
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