SLC30A10 Gene Hypermanganesemia With Dystonia Polycythemia And Cirrhosis NGS Genetic DNA Test cost NGN 400000
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SLC30A10 Gene Hypermanganesemia With Dystonia Polycythemia And Cirrhosis NGS Genetic DNA Test

Original price was: ₦ 560,000.Current price is: ₦ 400,000.

-29%

The SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test is a specialized genetic test that identifies mutations in the SLC30A10 gene, which can lead to hypermanganesemia and associated disorders. This test is crucial for patients showing symptoms of dystonia, polycythemia, and cirrhosis, providing insights into potential genetic causes and guiding treatment options. The test is available for 560,000 NGN, with a discounted price of 400,000 NGN.

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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 designed to identify genetic mutations associated with hypermanganesemia, a condition that can lead to serious neurological and metabolic disorders. This test utilizes Next Generation Sequencing (NGS) technology to analyze the SLC30A10 gene, providing critical insights into the genetic basis of various symptoms, including dystonia, polycythemia, and cirrhosis.

What the Test Measures

This test specifically detects mutations in the SLC30A10 gene, which is responsible for manganese transport in the body. Abnormalities in this gene can lead to elevated manganese levels, causing toxicity that affects the nervous system and other organs.

Who Should Consider This Test

Individuals experiencing symptoms such as:

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

Additionally, those with a family history of these conditions or other metabolic disorders should consider this test to uncover potential genetic predispositions.

Benefits of Taking the Test

  • Identifies genetic mutations that may be causing symptoms.
  • Guides treatment options and management of symptoms.
  • Provides valuable information for family planning and genetic counseling.
  • Enhances understanding of personal health risks associated with genetic conditions.

Understanding Your Results

Results from the SLC30A10 Gene Hypermanganesemia test will provide insights into whether mutations are present. A genetic counselor will assist in interpreting the results, discussing implications for treatment and lifestyle adjustments.

Test Pricing

Test Name Discount Price Regular Price
SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test 400,000 NGN 560,000 NGN

Book Your Test Today!

Don’t wait to take control of your health. Book the SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test now. For inquiries or to schedule an appointment, please call or WhatsApp us at +2348077798758.

Turnaround time for results is approximately 3 to 4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card. Pre-test instructions include a clinical history and a genetic counseling session to draw a pedigree chart of family members affected by the conditions mentioned.

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