KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test

Introduction

The KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test is a specialized diagnostic test designed to identify mutations in the KCNJ1 gene, which are associated with Bartter syndrome type 2. This condition affects the kidneys and can lead to various complications, including electrolyte imbalances and renal dysfunction. Early diagnosis through genetic testing is vital for effective management and treatment of the condition.

What the Test Measures

This test utilizes Next Generation Sequencing (NGS) technology to detect mutations in the KCNJ1 gene. These mutations can disrupt the normal function of ion channels in the kidneys, leading to the clinical manifestations of Bartter syndrome type 2.

Who Should Consider This Test

Individuals who exhibit symptoms such as:

• Frequent dehydration
• Muscle weakness or cramps
• Fatigue
• Low blood pressure
• High levels of potassium in urine

Additionally, those with a family history of Bartter syndrome or related genetic conditions should consider this test for early detection and management.

Benefits of Taking the Test

• Accurate diagnosis of Bartter syndrome type 2.
• Guides treatment decisions and management strategies.
• Helps in understanding the genetic basis of renal disorders.
• Provides valuable information for family planning and genetic counseling.

Understanding Your Results

Results from the KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test will indicate whether mutations are present in the KCNJ1 gene. A genetic counselor can help interpret these results and discuss their implications for treatment and family health.

Test Pricing

Our Services

We have branches across Kenya and offer home sample collection services for your convenience. To book your test or for more information, please call or WhatsApp us at +254746849631.

Don’t wait until symptoms worsen; take charge of your health today with the KCNJ1 Gene Bartter Syndrome Type 2 NGS Genetic DNA Test!