Diagnostic Utility of Genetic Testing in Hyperthyroxinemia With Non‐Suppressed TSH
Our findings highlight the critical role of molecular testing in accurately diagnosing the underlying cause of elevated FT4 with non-suppressed TSH and in preventing unnecessary interventions. Hotspot analysis of the ALB gene is recommended as a first-line test, particularly in asymptomatic individuals.
Authors
- Mehmet Eltan (ORCID: https://orcid.org/0000-0001-6977-9620)
- Şenol Demir (ORCID: https://orcid.org/0000-0002-8374-0359)
- Dilek Giray (ORCID: https://orcid.org/0000-0001-7660-4052)
- Saygin Abali
- Zehra Yavas Abali
- Hilal Sekizkardes
Institutions
- Education Training And Research (US)
- Sağlık Bilimleri Üniversitesi (TR)
- Kent Hastanesi (TR)
- Marmara University (TR)
- University of Health Sciences Antigua (AG)
Publication Details
- Journal
- Clinical Endocrinology
- Published
- 2026-03-09
- DOI
- https://doi.org/10.1111/cen.70126
- Primary Topic
- Thyroid Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00