Resistance to thyroid hormone in a family with no TRbeta gene anomaly: pathogenic hypotheses
| Autor: | V, Vlaeminck-Guillem, A, Margotat, J, Torresani, M, D'herbomez, M, Decoulx, J L, Wémeau |
|---|---|
| Rok vydání: | 2000 |
| Předmět: |
Adult
Thyroid Hormone Resistance Syndrome Receptors Thyroid Hormone Genetic Linkage Thyrotropin Sequence Analysis DNA Pedigree Thyroxine Haplotypes Mutation Humans Triiodothyronine Female Dinucleotide Repeats Thyrotropin-Releasing Hormone Polymorphism Restriction Fragment Length Polymorphism Single-Stranded Conformational |
| Zdroj: | Annales d'endocrinologie. 61(3) |
| ISSN: | 0003-4266 |
| Popis: | Syndromes of resistance to thyroid hormone (RTH) are almost always linked to a defective triiodothyronine-receptor B gene (TRB). Only six families with RTH exhibiting a normal TRB gene have been reported so far. We report another and discuss possible mechanisms.We studied a kindred expressing a typical RTH phenotype. DNA was amplified and the TRB gene was sequenced. Linkage analysis assessed linkage between the TRB gene and RTH phenotype.Direct sequencing of the TRB gene failed to identify any anomaly in the coding exons. Linkage analysis demonstrated that the RTH phenotype was not linked to the TRB gene in this family.TRB1 and TRB2 genes were not defective in this family. Multiple mechanisms might account for this situation at the pre-receptor, receptor and post-receptor levels. The most likely hypothesis is the involvement of an abnormal nuclear cofactor serving a specific function in the regulation of thyroid hormone action. |
| Databáze: | OpenAIRE |
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