TSH Receptor Gene Polymorphisms in Graves' Disease and Graves' Ophthalmopathy: Current Evidence, Molecular Mechanisms, and Clinical Implications

Authors

  • Farid Fawzy Abd El-Hafiz , Khalid Ahmed Ahmed Elbanna , Nermin Saad Ghanem, Norhan Abdallah Said Sabbah , Abdelhamid Moustafa Abdelhamid Elmougi Author

DOI:

https://doi.org/10.48047/j2mtan89

Keywords:

TSH Receptor Gene, Polymorphisms, Graves' Disease, Graves' Ophthalmopathy

Abstract

Background: Graves' disease (GD) is the most common cause of autoimmune hyperthyroidism and results from a complex interplay between genetic susceptibility, immune dysregulation, and environmental triggers. Among the numerous genetic loci implicated in disease pathogenesis, the thyroid-stimulating hormone receptor (

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References

Smith TJ, Hegedüs L. Graves' disease. N Engl J Med. 2016;375(16):1552-1565. doi:10.1056/NEJMra1510030

Lee HJ, Li CW, Hammerstad SS, Stefan M, Tomer Y. Immunogenetics of autoimmune thyroid diseases: A comprehensive review. J Autoimmun. 2015;64:82-90. doi:10.1016/j.jaut.2015.07.009

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Published

2024-11-20

How to Cite

TSH Receptor Gene Polymorphisms in Graves’ Disease and Graves’ Ophthalmopathy: Current Evidence, Molecular Mechanisms, and Clinical Implications (Farid Fawzy Abd El-Hafiz , Khalid Ahmed Ahmed Elbanna , Nermin Saad Ghanem, Norhan Abdallah Said Sabbah , Abdelhamid Moustafa Abdelhamid Elmougi , Trans.). (2024). Cuestiones De Fisioterapia, 53(03), 7730-7740. https://doi.org/10.48047/j2mtan89