SIK1 Gene Early Infantile Epileptic Encephalopathy Type 30 NGS Genetic DNA Test
Introduction
The SIK1 Gene Early Infantile Epileptic Encephalopathy Type 30 NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with early infantile epileptic encephalopathy, a severe neurological disorder affecting infants. This test is crucial for understanding the underlying genetic factors that contribute to the condition, enabling timely intervention and management.
What the Test Measures
This genetic test analyzes the SIK1 gene to detect mutations that may lead to early infantile epileptic encephalopathy type 30. By employing Next-Generation Sequencing (NGS) technology, it offers high sensitivity and specificity in identifying genetic variations.
Who Should Consider This Test?
Parents or guardians of infants displaying symptoms such as:
- Severe seizures
- Developmental delays
- Unexplained neurological issues
Additionally, families with a history of neurological disorders should consider this test to assess potential genetic risks.
Benefits of Taking the Test
- Early diagnosis of genetic causes of neurological disorders.
- Guides treatment decisions and management strategies.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the SIK1 Gene test will help in determining whether a genetic mutation is present. A genetic counseling session is recommended to interpret the results accurately and discuss the implications for the patient and family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SIK1 Gene Early Infantile Epileptic Encephalopathy Type 30 NGS Genetic DNA Test | KSh 40,000 | KSh 56,000 |
Branch Locations and Booking
We have branches across major cities in Kenya, including Nairobi, Mombasa, Kisumu, and more. For your convenience, we also offer home sample collection services.
To book the SIK1 Gene Early Infantile Epileptic Encephalopathy Type 30 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
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 create a pedigree chart of family members affected by the condition.
