| Literature DB >> 27758132 |
Chutintorn Sriphrapradang1, Panudda Srichomkwun2, Samuel Refetoff2,3,4, Sunee Mamanasiri5.
Abstract
A patient is reported with resistance to thyroid hormone beta caused by a novel THRB gene mutation and coexisting pituitary microadenoma. A 41-year-old Thai woman presented with elevated serum thyroid hormone levels and non-suppressed thyrotropin (TSH). Magnetic resonance imaging showed a 4 mm × 2 mm pituitary adenoma. Five of her relatives had similar thyroid tests abnormalities, but a sister had Graves' disease. Thyroperoxidase and thyroglobulin antibodies were positive in all affected family members, except for the proband's 4.5-year-old niece. Lack of thyrotoxic symptoms and TSH suppression by triiodothyronine indicated incidentaloma rather than a TSH-secreting pituitary adenoma. Genetic analysis revealed a THRB gene mutation (c.1037G>T), resulting in p.G251V.Entities:
Keywords: autoimmune diseases; inappropriate TSH secretion syndrome; mutation; pituitary tumor; thyroid hormone receptor; thyroid hormone resistance syndrome
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Year: 2016 PMID: 27758132 PMCID: PMC5175442 DOI: 10.1089/thy.2016.0450
Source DB: PubMed Journal: Thyroid ISSN: 1050-7256 Impact factor: 6.568