KCNQ1OT1 Gene Beckwith-Wiedemann Syndrome Genetic Test
Cost: AED 4400.0
Test Components:
- KCNQ1OT1 Gene Beckwith-Wiedemann Syndrome Genetic Test
Sample Condition:
Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery:
3 to 4 Weeks
Method:
NGS Technology (Next-Generation Sequencing)
Test Type:
Cancer
Doctor:
Oncologist
Test Department:
Genetics
Pre Test Information:
Clinical History of Patient who is going for KCNQ1OT1 Gene Beckwith-Wiedemann Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KCNQ1OT1 Gene Beckwith-Wiedemann Syndrome NGS Genetic DNA Test gene KCNQ1OT1.
Test Details:
The KCNQ1OT1 gene is associated with Beckwith-Wiedemann Syndrome (BWS), a rare genetic disorder characterized by overgrowth, abdominal wall defects, and an increased risk of developing certain tumors. NGS genetic testing is a method used to analyze the DNA sequence of a person’s genes to identify any mutations or abnormalities that may be present. A KCNQ1OT1 gene NGS genetic test specifically focuses on sequencing the KCNQ1OT1 gene to detect any mutations or variations that may be associated with BWS.
This test can help confirm a diagnosis of BWS in individuals who show symptoms of the disorder or have a family history of BWS. The results of the NGS genetic test can provide valuable information for healthcare providers in managing the individual’s condition and determining the appropriate treatment and monitoring options. It can also help in providing genetic counseling to individuals and their families regarding the risk of passing on the condition to future generations.
It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support throughout the testing process.
| Test Name | KCNQ1OT1 Gene Beckwith-Wiedemann syndrome 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 | Cancer |
| Doctor | Oncologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for KCNQ1OT1 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KCNQ1OT1 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test gene KCNQ1OT1 |
| Test Details |
The KCNQ1OT1 gene is associated with Beckwith-Wiedemann syndrome (BWS), a rare genetic disorder characterized by overgrowth, abdominal wall defects, and an increased risk of developing certain tumors. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes to identify any mutations or abnormalities that may be present. A KCNQ1OT1 gene NGS genetic test specifically focuses on sequencing the KCNQ1OT1 gene to detect any mutations or variations that may be associated with BWS. This test can help confirm a diagnosis of BWS in individuals who show symptoms of the disorder or have a family history of BWS. The results of the NGS genetic test can provide valuable information for healthcare providers in managing the individual’s condition and determining the appropriate treatment and monitoring options. It can also help in providing genetic counseling to individuals and their families regarding the risk of passing on the condition to future generations. It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support throughout the testing process. |
