F7 Gene Factor VII deficiency Genetic Test
Genetic testing plays a crucial role in understanding various genetic disorders and their implications. In this blog, we will discuss the F7 Gene Factor VII deficiency Genetic Test offered by DNA Labs UAE.
Test Name: F7 Gene Factor VII deficiency 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: Vascular Diseases
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information:
Before undergoing the F7 Gene Factor VII deficiency NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by the F7 Gene Factor VII deficiency NGS Genetic DNA Test gene F7.
Test Details:
The F7 Gene Factor VII deficiency NGS Genetic Test is a genetic test that utilizes next-generation sequencing (NGS) technology to analyze the F7 gene for mutations or variations associated with Factor VII deficiency. Factor VII deficiency is a rare bleeding disorder that affects the blood’s ability to clot properly.
The F7 gene provides instructions for producing a protein called Factor VII, which plays a crucial role in the blood clotting process. Mutations or variations in the F7 gene can result in reduced levels or impaired function of Factor VII, leading to abnormal bleeding.
The NGS genetic test involves collecting a sample of DNA, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to examine the entire F7 gene for any genetic changes. These changes can include single nucleotide variants (SNVs), insertions, deletions, or other structural variations.
By identifying specific mutations or variations in the F7 gene, the test can aid in diagnosing Factor VII deficiency and determining the genetic cause of the condition. This information can be valuable for genetic counseling, family planning, and potentially guiding treatment decisions.
It is important to note that a positive genetic test result does not necessarily mean that an individual will develop symptoms of Factor VII deficiency. The severity and presentation of the condition can vary widely, and additional factors beyond genetics can influence the risk and clinical manifestation of the disorder.
Therefore, genetic testing should always be interpreted in the context of a person’s clinical symptoms and family history.
| Test Name | F7 Gene Factor VII deficiency 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 | Vascular Diseases |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for F7 Gene Factor VII deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F7 Gene Factor VII deficiency NGS Genetic DNA Test gene F7 |
| Test Details | F7 Gene Factor VII deficiency NGS Genetic Test is a genetic test that uses next-generation sequencing (NGS) technology to analyze the F7 gene for mutations or variations that may be associated with Factor VII deficiency. Factor VII deficiency is a rare bleeding disorder that affects the blood’s ability to clot properly. The F7 gene provides instructions for making a protein called Factor VII, which plays a crucial role in the blood clotting process. Mutations or variations in the F7 gene can lead to reduced levels or impaired function of Factor VII, resulting in abnormal bleeding. The NGS genetic test involves collecting a sample of DNA, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to examine the entire F7 gene for any genetic changes. These changes can include single nucleotide variants (SNVs), insertions, deletions, or other structural variations. By identifying specific mutations or variations in the F7 gene, the test can help diagnose Factor VII deficiency and determine the genetic cause of the condition. This information can be useful for genetic counseling, family planning, and potentially guiding treatment decisions. It is important to note that a positive genetic test result does not necessarily mean that an individual will develop symptoms of Factor VII deficiency. The severity and presentation of the condition can vary widely, and additional factors beyond genetics can influence the risk and clinical manifestation of the disorder. Therefore, genetic testing should always be interpreted in the context of a person’s clinical symptoms and family history. |
