WNT3 Gene Tetraamelia Autosomal Recessive NGS Genetic DNA Test
Introduction
The WNT3 Gene Tetraamelia Autosomal Recessive NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with Tetraamelia, a rare congenital condition characterized by the absence of limbs. This test is crucial for early diagnosis and management of genetic disorders, particularly in pediatric patients.
What the Test Measures
This genetic test specifically analyzes the WNT3 gene using Next-Generation Sequencing (NGS) technology. It detects mutations that may lead to dysmorphology, allowing healthcare providers to understand the genetic underpinnings of the condition.
Who Should Consider This Test
Parents or guardians of children exhibiting symptoms such as limb malformations or other congenital anomalies should consider this test. Additionally, individuals with a family history of Tetraamelia or related genetic disorders may also benefit from this diagnostic tool.
Benefits of Taking the Test
- Early detection of genetic conditions in children.
- Informed decision-making regarding treatment options.
- Access to genetic counseling and support services.
- Understanding the risk of recurrence in future pregnancies.
Understanding Your Results
Results from the WNT3 Gene Tetraamelia test will help determine if a genetic mutation is present. A genetic counselor will assist in interpreting the results and discussing potential implications for the patient and family.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
WNT3 Gene Tetraamelia Autosomal Recessive NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Availability
We have branches across major cities in Kenya and offer a convenient home sample collection service. To book the WNT3 Gene Tetraamelia Autosomal Recessive NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Pre-Test Instructions
Before undergoing the WNT3 Gene Tetraamelia test, patients are required to provide a clinical history. A genetic counseling session is recommended to create a pedigree chart of family members affected by the WNT3 gene mutation.
Turnaround Time
The results for this test are typically available within 3 to 4 weeks.