HEREDITARY ENDOMETRIAL CANCER: CLINICAL EXOME PANEL (Sec. & CNVs) – 13 genes

LabGenetics
Caja de HEREDITARY ENDOMETRIAL CANCER: CLINICAL EXOME PANEL (Sec. & CNVs) – 13 genes

Delivery time

3-4 weeks

Sample

Blood

850,00€
Caja de HEREDITARY ENDOMETRIAL CANCER: CLINICAL EXOME PANEL (Sec. & CNVs) – 13 genes

The Hereditary Endometrial Cancer Panel identifies pathogenic variants in genes associated with a higher genetic predisposition to developing endometrial carcinoma. This type of cancer can be part of hereditary syndromes such as Lynch syndrome (HNPCC) or Cowden syndrome, and is also linked to mutations in DNA repair genes or tumor suppressor genes. Early detection of these alterations is essential for establishing personalized gynecological follow-up, defining preventive strategies, and guiding family genetic counseling. Genes analyzed: MLH1, MSH2, MSH6, PMS2, BRCA1, PTEN, TP53, and others. You can consult the complete list of analyzed genes by contacting Genotica.

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