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ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test

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

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The ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test is crucial for diagnosing neurological disorders. Priced at 560,000 NGN, this test utilizes advanced NGS technology to analyze genetic variations associated with hemiplegia. Understanding your genetic predisposition can lead to better management and treatment options. Book your test today!

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ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test

Introduction

The ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test is a vital diagnostic tool that helps in identifying genetic mutations associated with neurological disorders, specifically Alternating Hemiplegia of Childhood (AHC). This condition is characterized by recurrent episodes of hemiplegia, which can significantly impact a child’s development and quality of life. Understanding the genetic basis of AHC is crucial for effective management and treatment.

What the Test Measures

This test utilizes Next-Generation Sequencing (NGS) technology to detect mutations in the ATP1A3 gene, which plays a critical role in neuronal function. By analyzing the genetic material, healthcare providers can identify specific variations that may contribute to the development of AHC.

Who Should Consider This Test

Parents and guardians should consider this test if their child exhibits symptoms such as:

  • Recurrent episodes of weakness or paralysis on one side of the body
  • Difficulty with coordination and balance
  • Developmental delays or cognitive impairments
  • Family history of neurological disorders

Consultation with a neurologist is recommended to assess the need for testing based on clinical symptoms and family history.

Benefits of Taking the Test

  • Accurate diagnosis of Alternating Hemiplegia of Childhood
  • Informed treatment decisions based on genetic findings
  • Potential for early intervention and management strategies
  • Understanding the hereditary nature of the condition for family planning

Understanding Your Results

After the test is completed, results will be interpreted by a genetic counselor or neurologist. They will discuss the implications of the findings, including whether a mutation was detected and what it means for the child’s health and treatment options. It is essential to understand that not all genetic variations lead to disease, and professional guidance is crucial in interpreting results.

Test Information

Test Name Discount Price Regular Price
ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test 400,000 NGN 560,000 NGN

Book the Test Today!

To gain insights into your child’s neurological health, book the ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic DNA Test today. Contact us at +2348110567037 or visit our website to schedule your appointment. Take the first step towards understanding and managing your child’s health.