Book Lynch Syndrome Screening in Saudi Arabia | Lahalak Medical Platform

A vital screening that identifies genetic predispositions to cancers, enabling a personalized preventive plan for you and your family while ensuring optimal medical care and continuous monitoring.

Scientific name: Lynch Syndrome Screening for Endometrial Cancer

A specialized laboratory test performed on endometrial tissue specimens to detect DNA mismatch repair (MMR) deficiency using immunohistochemistry or advanced genetic testing methods for accurate diagnosis.

Lynch Syndrome Screening for Endometrial Cancer - Screening for Genetic Lynch Syndrome
Service type Genetic Laboratory Test
Duration 3-5 working days
Fasting Fasting is not required

Included Services

  • Immunohistochemistry (IHC) analysis
  • Detailed diagnostic report
  • Result consultation

Medical Service Information

Purpose of the Procedure

  • Identifying genetic predisposition to colon and endometrial cancers
  • Assessing cancer risks for other family members
  • Guiding appropriate treatment options based on genetic results

Target Groups

  • Patients diagnosed with endometrial cancer at a young age
  • Individuals with a strong family history of Lynch-associated cancers
  • Cases showing mismatch repair (MMR) protein deficiency

Frequently Asked Questions

  • Is the test painful? No, the test is performed on a previously collected tissue specimen (biopsy).
  • Are the results final? The screening is a strong indicator and may require supplemental genetic testing for confirmation.

Conditions & Notices

  • Endometrial tissue specimen is required
  • Previous medical reports are recommended

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