Book PJS Genetic Counseling in Saudi Arabia | Lahalak Medical Platform

Gain a comprehensive evaluation of hereditary Peutz-Jeghers Syndrome risks. We help you understand STK11 gene mutations and design a precise clinical surveillance plan to ensure early detection and protect your family's health.

Scientific name: Genetic Counseling for Peutz-Jeghers Syndrome (PJS)

A specialized counseling session to analyze medical history, explain STK11 genetic test results, and coordinate routine screening for bowel, breast, and pancreatic cancers associated with Peutz-Jeghers Syndrome.

Genetic Counseling for Peutz-Jeghers Syndrome (PJS) - Manage Hereditary Cancer Risk Early
Service type Medical Consultation
Duration 30-45 minutes
Fasting Fasting is not required

Included Services

  • Family history review
  • STK11 result interpretation
  • Surveillance recommendations

Medical Service Information

Purpose of Counseling

  • Assess the risk of cancers associated with the syndrome.
  • Interpret STK11 gene mutation test results.
  • Establish a timeline for preventive periodic screenings.

Who Should Attend?

  • Individuals with a family history of PJS.
  • Patients with characteristic freckling on lips or oral mucosa.
  • People with a history of recurrent intestinal polyps.

Importance of Surveillance

  • Early detection of bowel and pancreatic cancers.
  • Reducing the need for emergency surgical interventions.
  • Providing genetic guidance for other family members.

Conditions & Notices

  • Bring previous medical reports
  • Detailed family medical history

Medical services you might also like