Noonan RASophathies Panel NGS Genetic DNA Test

Introduction

The Noonan RASophathies Panel NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with Noonan syndrome and related disorders. This test employs Next-Generation Sequencing (NGS) technology to analyze specific genes that are known to contribute to these conditions. Early detection is crucial for effective management and treatment, making this test an important resource for patients and healthcare providers.

What the Test Measures

This genetic test measures mutations in genes such as BRAF, CBL, HRAS, KAT6B, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NF2, NRAS, PTPN11, RAF1, RASA2, RIT1, SHOC2, SMARCB1, SOS1, SOS2, SPRED1, TSC1, and TSC2. These genes are linked to various dysmorphological features and developmental disorders.

Who Should Consider This Test

Individuals who exhibit symptoms such as unusual facial features, heart defects, growth delays, or developmental delays should consider this test. Additionally, those with a family history of Noonan syndrome or related conditions may also benefit from testing.

Benefits of Taking the Test

• Accurate diagnosis of Noonan syndrome and related disorders.
• Informed decision-making regarding treatment and management.
• Family planning and genetic counseling opportunities.
• Access to specialized healthcare services tailored to the patient’s needs.

Understanding Your Results

Results are typically available within 3 to 4 weeks. A genetic counselor will help interpret the results, providing insights into the implications of any identified mutations and guiding further management strategies.

Test Pricing

Branches and Booking

We have branches across all major cities in Kenya, making it convenient for you to access our services. To book the Noonan RASophathies Panel NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Our team is ready to assist you with any inquiries and to schedule your appointment.