SI Gene Sucrase-Isomaltase Deficiency NGS Genetic DNA Test
Introduction to the SI Gene Sucrase-Isomaltase Deficiency NGS Genetic DNA Test
The SI Gene Sucrase-Isomaltase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies genetic mutations associated with sucrase-isomaltase deficiency. This metabolic disorder affects carbohydrate digestion, leading to various gastrointestinal symptoms. Understanding your genetic makeup can provide crucial insights into your health and guide effective management strategies.
What the Test Measures
This test specifically measures the presence of mutations in the SI gene, which encodes the sucrase-isomaltase enzyme. By utilizing Next-Generation Sequencing (NGS) technology, the test can detect even the most subtle genetic variations that may contribute to the deficiency.
Who Should Consider This Test?
Individuals experiencing symptoms such as:
- Chronic diarrhea
- Bloating and gas
- Abdominal pain after consuming sugars
Additionally, those with a family history of metabolic disorders or unexplained gastrointestinal issues should consider this test for a comprehensive evaluation.
Benefits of Taking the Test
- Accurate identification of genetic predisposition to sucrase-isomaltase deficiency.
- Guides dietary management and treatment plans.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the SI Gene Sucrase-Isomaltase Deficiency NGS Genetic DNA Test will indicate whether mutations are present. A genetic counselor will help interpret these results, providing insights into what they mean for your health and necessary next steps.
Test Pricing
| Discount Price | 400000 NGN |
|---|---|
| Regular Price | 560000 NGN |
Booking Your Test
To book the SI Gene Sucrase-Isomaltase Deficiency NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Our team is ready to assist you in understanding your health better!
Pre-Test Instructions
Before taking the test, ensure you have a clinical history prepared. A genetic counseling session is recommended to draw a pedigree chart of family members affected by sucrase-isomaltase deficiency.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
