Cep63 Gene Microcephaly Cep63 Related NGS Genetic DNA Test
Introduction to the Cep63 Gene Microcephaly Test
The Cep63 Gene Microcephaly Cep63 Related NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the CEP63 gene, which are linked to microcephaly and related disorders. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results. Understanding the genetic basis of microcephaly is essential for early diagnosis, intervention, and family planning.
What the Test Measures
This test detects mutations in the CEP63 gene, which can lead to microcephaly, a condition characterized by an abnormally small head and potential developmental delays. By analyzing the genetic material, healthcare providers can determine if a child is at risk for this condition.
Who Should Consider This Test
Parents with a family history of microcephaly, developmental delays, or other related disorders should consider this test. Symptoms such as developmental delays, unusual head size, and other neurological issues may indicate the need for genetic testing. Additionally, expectant parents with concerns about genetic disorders may find this test beneficial.
Benefits of Taking the Test
- Early diagnosis of potential genetic disorders.
- Informed family planning and reproductive choices.
- Access to tailored medical care and interventions.
- Peace of mind for families concerned about genetic conditions.
Understanding Your Results
Results from the Cep63 Gene Microcephaly Test will indicate whether a mutation is present in the CEP63 gene. A positive result may suggest a higher risk for microcephaly, while a negative result can provide reassurance. It is important to discuss the results with a healthcare professional who can provide guidance and support.
Test Pricing
| Price Type | Price (NGN) |
|---|---|
| Discount Price | 400000 NGN |
| Regular Price | 560000 NGN |
Book the Test
To book the Cep63 Gene Microcephaly Cep63 Related NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any questions you may have.
Test Details
- 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 and a genetic counselling session to draw a pedigree chart of family members affected with the CEP63 gene.
This test falls under the specialty of Pediatrics and the department of Genetics, utilizing NGS Technology to provide accurate results for the disease type of Dysmorphology.
