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SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test

Original price was: KSh 56,000.00.Current price is: KSh 40,000.00.

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The SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test is essential for diagnosing metabolic disorders related to manganese accumulation. Priced at KSh 56,000, this test is crucial for patients exhibiting symptoms like dystonia and polycythemia. We provide home sample collection across Kenya, ensuring convenience and accessibility. Get tested today!

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SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test
SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test
KSh 56,000.00 Original price was: KSh 56,000.00.KSh 40,000.00Current price is: KSh 40,000.00.

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SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test

Introduction

The SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test is a cutting-edge diagnostic tool that plays a pivotal role in identifying metabolic disorders associated with manganese accumulation. This test utilizes Next-Generation Sequencing (NGS) technology to analyze the SLC30A10 gene, which is critical for manganese transport in the body. Early detection through this test can lead to better management of symptoms and improved patient outcomes.

What the Test Measures

This genetic test measures mutations in the SLC30A10 gene, which can lead to conditions such as hypermanganesemia, dystonia, polycythemia, and cirrhosis. By identifying these mutations, healthcare providers can better understand the underlying causes of the patient’s symptoms.

Who Should Consider This Test

Individuals experiencing symptoms such as:

  • Dystonia (involuntary muscle contractions)
  • Polycythemia (increased red blood cell mass)
  • Cirrhosis (liver scarring)

Patients with a family history of these conditions or those who have been diagnosed with related metabolic disorders should consider this test. Risk factors include genetic predisposition and environmental exposure to manganese.

Benefits of Taking the Test

  • Accurate diagnosis of metabolic disorders.
  • Guidance for treatment options based on genetic findings.
  • Early intervention can improve quality of life.
  • Informed family planning through genetic counseling.

Understanding Your Results

Results from the SLC30A10 Gene Hypermanganesemia test will provide insights into whether mutations are present in the SLC30A10 gene. A genetic counselor will help interpret these results and discuss the implications for treatment and management.

Test Name and Price

Price Type Price (KSh)
Discount Price 40,000
Regular Price 56,000

Convenience Across Kenya

We have branches across all major cities in Kenya including Nairobi, Mombasa, and Kisumu. For added convenience, we offer home sample collection services to ensure you can get tested without hassle.

Book Your Test Today!

Don’t wait to get the answers you need. Book the SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test today! For more information or to schedule your appointment, call or WhatsApp us at +254711564616.