HEREDITARY THYROID CANCER: CLINICAL EXOME PANEL (Sec. & CNVs) – 17 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
The Hereditary Thyroid Cancer Panel is designed to identify genetic variants responsible for the main syndromes associated with medullary, papillary, and follicular thyroid carcinoma. It includes genes involved in tumor predisposition syndromes such as MEN2 syndrome (RET), Cowden syndrome (PTEN), Carney syndrome (PRKAR1A), and alterations in APC and DICER1 related to thyroid tumors and other multiple endocrine neoplasms. This analysis is essential for early diagnosis, family management, and prevention of hereditary endocrine neoplasms. Genes analyzed: RET, PTEN, APC, PRKAR1A, CHEK2, DICER1, SDHB, SDHD, TP53, and others. You can consult the complete list of analyzed genes by contacting Genotica.
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