Book Lynch Syndrome Genetic Test | Lahalak Medical Platform

Discover hereditary risks for endometrial and colon cancer early. Lynch syndrome screening helps you make informed preventive health decisions for yourself and your family with expert genomic guidance and monitoring.

Scientific name: Lynch Syndrome (HNPCC) Genetic Screening

Advanced genetic screening for MMR gene mutations associated with endometrial and colorectal cancers. It assesses hereditary risks to ensure precise medical monitoring and prevention for high-risk pregnancies.

Lynch Syndrome (HNPCC) Genetic Screening - Protect Your Family from Hereditary Cancer
Service type Genetic Laboratory Test
Duration 10-15 minutes
Fasting Fasting is not required

Included Services

  • Blood sample collection
  • Gene sequencing (MLH1, MSH2, MSH6, PMS2)
  • Detailed medical report

Medical Service Information

Purpose of the Screening

  • Identify hereditary risk for endometrial and ovarian cancers.
  • Detect mutations in DNA mismatch repair (MMR) genes.
  • Establish a precise monitoring plan for high-risk pregnancies.

Who Should Get Tested?

  • Women with a family history of colon or endometrial cancer.
  • Patients previously diagnosed with Lynch-related tumors.
  • Pregnant women requiring high-risk care due to genetic factors.

Genes Included

  • MLH1 Gene
  • MSH2 Gene
  • MSH6 Gene
  • PMS2 Gene

Conditions & Notices

  • Providing family medical history is preferred

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