Genodiagnostics of MEN 1, 2A, 2B syndrome and familial thyroid cancer (MEN (2 exons) and RET (6 exons))

Pathogenic mutations in the 2nd and 10th exons of the MEN1 gene cause the development of multiple endocrine neoplasia type 1, a hereditary autosomal dominant disease. Pathogenic mutations in the 10th, 11th, 13-16th exons of the RET gene cause the development of multiple endocrine neoplasia type 2, a hereditary autosomal dominant disease.

Within 11 days. The specified time does not include the day of biomaterial collection