Book Wilms Tumor Genetic Consultation | Lahalak Medical Platform

Specialized consultation to evaluate genetic risks associated with Wilms tumor, aimed at early detection of predisposing syndromes to ensure a comprehensive preventive plan for your child's health and future.

Scientific name: Genetic Risk Consultation for Wilms Tumor

Comprehensive clinical and genetic evaluation for syndromes predisposing to Wilms tumor, such as WAGR or Beckwith-Wiedemann, helping families understand hereditary risks and determine necessary follow-up steps.

Genetic Risk Consultation for Wilms Tumor - Assess Your Child's Genetic Risk
Service type Medical Consultation
Duration 30-45 minutes
Fasting Fasting is not required

Included Services

  • Medical and family history review
  • Clinical evaluation of physical markers
  • Genetic laboratory testing recommendations

Medical Service Information

Consultation Goals

  • Determine the likelihood of developing Wilms tumor based on genetics.
  • Screen for syndromes like WAGR and Beckwith-Wiedemann.
  • Establish a timeline for periodic screening and early detection.

Who Should Get This?

  • Children with congenital growth-related defects.
  • Families with a history of pediatric kidney tumors.
  • Cases suspected of having overgrowth syndromes.

Frequently Asked Questions

  • Does the consultation require a blood sample? It is an evaluation that may lead to a genetic blood test.
  • Is Wilms tumor always hereditary? No, but a percentage of cases are linked to specific genetic syndromes.

Conditions & Notices

  • Bring all previous medical reports for the child
  • Preferably both parents should attend the consultation

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