ATR Gene Seckel syndrome type 1 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 ATR Gene Seckel syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ATR Gene Seckel syndrome type 1 NGS Genetic DNA Test gene ATR.
Test Details:
The ATR gene is associated with Seckel syndrome type 1, a rare genetic disorder characterized by growth delays, intellectual disability, and distinctive facial features. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of the ATR gene and identify any mutations or variations that may be present. This test can help confirm a diagnosis of Seckel syndrome type 1 and provide information about the specific genetic cause of the condition. It may also be used for carrier testing in families with a known history of Seckel syndrome type 1.
Test Name | ATR Gene Seckel syndrome type 1 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 ATR Gene Seckel syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ATR Gene Seckel syndrome type 1 NGS Genetic DNA Test gene ATR |
Test Details |
The ATR gene is associated with Seckel syndrome type 1, a rare genetic disorder characterized by growth delays, intellectual disability, and distinctive facial features. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of the ATR gene and identify any mutations or variations that may be present. This test can help confirm a diagnosis of Seckel syndrome type 1 and provide information about the specific genetic cause of the condition. It may also be used for carrier testing in families with a known history of Seckel syndrome type 1. |