CYP24A1 Gene Hypercalcemia Infantile Type NGS Genetic DNA Test
Introduction
The CYP24A1 Gene Hypercalcemia Infantile Type NGS Genetic DNA Test is a crucial diagnostic tool designed to identify genetic mutations associated with hypercalcemia in infants. This condition, characterized by elevated calcium levels in the blood, can lead to severe health complications if not diagnosed and managed promptly. Utilizing Next Generation Sequencing (NGS) technology, this test provides a comprehensive analysis of the CYP24A1 gene, enabling early detection and intervention.
What the Test Measures
This genetic test specifically measures mutations in the CYP24A1 gene, which plays a significant role in calcium metabolism. By analyzing the genetic code, healthcare providers can determine the presence of hereditary conditions that may contribute to hypercalcemia.
Who Should Consider This Test?
Infants exhibiting symptoms of hypercalcemia, such as:
- Excessive thirst and urination
- Constipation
- Lethargy
- Bone pain or weakness
- Growth delays
Additionally, infants with a family history of metabolic disorders or those who have undergone genetic counseling should consider this test.
Benefits of Taking the Test
- Early identification of genetic causes of hypercalcemia.
- Informed decision-making regarding treatment options.
- Guidance for family planning and genetic counseling.
- Accurate diagnosis to prevent further health complications.
Understanding Your Results
Results from the CYP24A1 Gene Hypercalcemia Infantile Type NGS Genetic DNA Test typically take 3 to 4 weeks. Your healthcare provider will discuss the findings with you, helping you understand the implications of any detected mutations and the next steps for management.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CYP24A1 Gene Hypercalcemia Infantile Type NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across major cities in Kenya, including Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. To book the CYP24A1 Gene Hypercalcemia Infantile Type NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Pre-Test Instructions
Before undergoing the test, it is essential to provide a clinical history of the patient. A genetic counseling session is recommended to draw a pedigree chart of family members affected by hypercalcemia infantile type.
