CEP63 Gene Seckel syndrome type 6 Genetic Test
Components
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for CEP63 Gene Seckel syndrome type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CEP63 Gene Seckel syndrome type 6 NGS Genetic DNA Test gene CEP63.
Test Details
The CEP63 gene is associated with Seckel syndrome type 6, which is a rare genetic disorder characterized by growth retardation, microcephaly (small head size), and intellectual disability. The NGS genetic test refers to Next-Generation Sequencing, which is a high-throughput method used to analyze multiple genes simultaneously.
The NGS genetic test for CEP63 gene mutations involves sequencing the entire coding region of the gene to identify any genetic variations or mutations that may be causing Seckel syndrome type 6. This test can help confirm a diagnosis and provide information about the specific genetic changes responsible for the disorder.
NGS genetic testing for CEP63 gene mutations can be performed on a blood or saliva sample. The sample is sent to a specialized laboratory where the DNA is extracted and sequenced. The sequencing data is then analyzed to identify any variations or mutations in the CEP63 gene.
The results of the NGS genetic test can help in genetic counseling, family planning, and potentially guide treatment decisions. It is important to consult with a genetic counselor or healthcare provider to understand the implications of the test results and discuss any further steps or recommendations.
| Test Name | CEP63 Gene Seckel syndrome type 6 Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Dysmorphology |
| Doctor | Pediatrics |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for CEP63 Gene Seckel syndrome type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CEP63 Gene Seckel syndrome type 6 NGS Genetic DNA Test gene CEP63 |
| Test Details |
The CEP63 gene is associated with Seckel syndrome type 6, which is a rare genetic disorder characterized by growth retardation, microcephaly (small head size), and intellectual disability. The NGS genetic test refers to Next-Generation Sequencing, which is a high-throughput method used to analyze multiple genes simultaneously. The NGS genetic test for CEP63 gene mutations involves sequencing the entire coding region of the gene to identify any genetic variations or mutations that may be causing Seckel syndrome type 6. This test can help confirm a diagnosis and provide information about the specific genetic changes responsible for the disorder. NGS genetic testing for CEP63 gene mutations can be performed on a blood or saliva sample. The sample is sent to a specialized laboratory where the DNA is extracted and sequenced. The sequencing data is then analyzed to identify any variations or mutations in the CEP63 gene. The results of the NGS genetic test can help in genetic counseling, family planning, and potentially guide treatment decisions. It is important to consult with a genetic counselor or healthcare provider to understand the implications of the test results and discuss any further steps or recommendations. |
