NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test

Introduction

The NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the NRAS gene, which are associated with Noonan Syndrome. This condition is characterized by a range of developmental issues and physical anomalies. Understanding the genetic basis of this syndrome is crucial for effective management and treatment, especially in pediatric patients.

What the Test Measures

This test utilizes Next-Generation Sequencing (NGS) technology to detect specific mutations in the NRAS gene. By analyzing the genetic material from a blood sample or extracted DNA, healthcare providers can gain insights into the presence of genetic variations that may lead to Noonan Syndrome.

Who Should Consider This Test

Individuals who should consider the NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test include:

• Children exhibiting symptoms of Noonan Syndrome, such as distinct facial features, heart defects, and growth delays.
• Families with a history of Noonan Syndrome or related genetic conditions.
• Patients with a clinical history suggestive of dysmorphology.

Benefits of Taking the Test

• Early diagnosis can lead to timely interventions and management strategies.
• Provides valuable information for family planning and genetic counseling.
• Helps in understanding the risk of recurrence in future pregnancies.

Understanding Your Results

Once the test is completed, results will be analyzed and shared with the patient or guardian. It is important to consult with a healthcare professional for a comprehensive interpretation of the results. The results can guide further management and treatment options for affected individuals.

Test Pricing

Booking the Test

We have branches across Kenya, including Nairobi, Mombasa, and Kisumu, and offer a convenient home sample collection service. To book the NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.