PDHX Gene Lacticacidemia Due To PDX1 Deficiency NGS Genetic DNA Test
Introduction to the Test
The PDHX Gene Lacticacidemia due to PDX1 deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with lacticacidemia, a serious metabolic disorder. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive genetic insights, which are crucial for early diagnosis and management of the condition.
What the Test Measures
This genetic test specifically measures variations in the PDHX gene, which plays a pivotal role in the metabolic pathway. By identifying mutations in this gene, healthcare providers can assess the risk of lacticacidemia and guide appropriate treatment plans.
Who Should Consider This Test?
Individuals who exhibit symptoms of metabolic disorders, particularly those related to energy production and lactic acid accumulation, should consider this test. Risk factors include:
- Family history of metabolic disorders
- Symptoms such as muscle weakness, fatigue, or neurological issues
- Unexplained metabolic acidosis
Benefits of Taking the Test
- Early identification of genetic predisposition to lacticacidemia
- Informed decision-making regarding treatment options
- Ability to guide family planning and genetic counseling
- Improved management of symptoms and overall health
Understanding Your Results
Results from the PDHX Gene Lacticacidemia due to PDX1 deficiency NGS Genetic DNA Test will provide insights into whether genetic mutations are present. It is essential to discuss these results with a qualified healthcare provider, who can help interpret the findings and recommend appropriate next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test Today!
To ensure timely diagnosis and intervention, book your PDHX Gene Lacticacidemia due to PDX1 deficiency NGS Genetic DNA Test today! For appointments, please call or WhatsApp us at +2348077798758. Take the first step towards understanding your health!
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required along with a genetic counseling session to draw a pedigree chart of family members affected with lacticacidemia due to PDX1 deficiency.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders
