PCK1 Gene Phosphoenolpyruvate Carboxykinase Deficiency Cytosolic NGS Genetic DNA Test
The PCK1 Gene Phosphoenolpyruvate Carboxykinase Deficiency Cytosolic NGS Genetic DNA Test is an advanced diagnostic tool that plays a vital role in identifying genetic mutations associated with metabolic disorders. Understanding your genetic makeup is essential for personalized healthcare, especially for conditions related to the PCK1 gene.
What the Test Measures/Detects
This genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the PCK1 gene, which is crucial for glucose metabolism. It detects mutations and variations in the gene that may lead to phosphoenolpyruvate carboxykinase deficiency, a rare metabolic disorder.
Who Should Consider This Test?
Individuals who exhibit symptoms such as hypoglycemia, metabolic acidosis, or have a family history of metabolic disorders should consider taking this test. Risk factors include:
- Family history of PCK1 gene mutations
- Symptoms of metabolic dysfunction
- Previous diagnoses of related metabolic disorders
Benefits of Taking the Test
Taking the PCK1 Gene test offers numerous benefits, including:
- Accurate diagnosis of metabolic disorders
- Informed decision-making regarding treatment options
- Identification of at-risk family members
- Guidance for dietary and lifestyle adjustments
Understanding Your Results
Results from the PCK1 Gene test will provide insights into any genetic mutations present. A genetic counseling session is recommended to help interpret the results and discuss potential implications for you and your family.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| PCK1 Gene Phosphoenolpyruvate Carboxykinase Deficiency Cytosolic NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the PCK1 Gene Phosphoenolpyruvate Carboxykinase Deficiency Cytosolic NGS Genetic DNA Test today for just 400,000 NGN. For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected with phosphoenolpyruvate carboxykinase deficiency.
Specialty: General Physician | Department: Genetics | Method: NGS Technology | Disease Type: Metabolic Disorders
