ArticleCureus2025
Thyroid Hormone Resistance: A Case Report of a Novel Missense Thyroid Hormone Receptor (THR) Mutation.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Resistance to thyroid hormone is a rare genetic condition caused by germline mutations of the thyroid hormone receptor gene. The precise incidence is unknown; sporadic or de novo mutations are found. The mutant receptor results in an impaired thyroid hormone function. Thyroid hormone receptor beta gene (THRB) mutations and alpha gene (THRA) mutations are the main sites of mutation. Clinical features vary; they can show features of hyperthyroidism, hypothyroidism, or a combination of both. Even different tissues in the same individual may have different effects. Diagnosis is confirmed by genetic testing. The treatment is based on symptoms. Here we describe a case of thyroid hormone resistance, whose case was confirmed with genetic analysis, with a mutation in the THR gene, not found on online databases.
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