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PROS1 Gene Protein S Deficiency Autosomal Dominant Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The PROS1 gene is responsible for the production of Protein S, a crucial anticoagulant in the human body that helps prevent excessive blood clotting. A deficiency in Protein S can lead to an increased risk of developing dangerous blood clots, a condition that can manifest in various serious health issues, including deep vein thrombosis and pulmonary embolism. This condition is often inherited in an autosomal dominant manner, meaning that only one copy of the altered gene in each cell is sufficient to cause the disorder.

To diagnose Protein S deficiency linked to the PROS1 gene, a genetic test is available. This test is designed to identify mutations in the PROS1 gene that could lead to Protein S deficiency. Conducted at DNA Labs UAE, the genetic test is a critical tool for individuals with a family history of blood clotting disorders or those who have experienced unexplained thrombotic events. Early detection through this test can be instrumental in managing the condition, implementing preventive measures, and reducing the risk of complications associated with excessive blood clotting.

The cost of the PROS1 gene Protein S deficiency autosomal dominant genetic test at DNA Labs UAE is 4400 AED. This investment in health allows individuals to gain valuable insights into their genetic makeup, empowering them with the knowledge to take proactive steps in managing their health and preventing potential blood clotting disorders.

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PROS1 Gene Protein S Deficiency autosomal dominant Genetic Test

Test Details

Pros1 gene protein S deficiency is a genetic disorder that affects the production or function of protein S, a protein that plays a critical role in preventing blood clot formation. Autosomal dominant inheritance means that a person only needs to inherit one copy of the defective gene from either parent to develop the condition.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes. When it comes to Pros1 gene protein S deficiency, NGS genetic testing offers several advantages:

  1. Comprehensive analysis: NGS can analyze multiple genes simultaneously, providing a comprehensive evaluation of the genetic basis of protein S deficiency. This can help identify other potential genetic factors contributing to the disorder and rule out other related conditions.
  2. Cost-effective: NGS allows for the analysis of multiple genes in a single test, making it more cost-effective compared to traditional Sanger sequencing, which analyzes genes one at a time.
  3. Time-efficient: NGS can analyze a large number of genes within a relatively short period, providing quicker results compared to traditional sequencing methods.
  4. Increased diagnostic yield: NGS has a higher diagnostic yield compared to traditional methods, as it can detect a wider range of genetic variations, including single nucleotide variants, insertions, deletions, and structural rearrangements.
  5. Personalized treatment: NGS can help identify specific genetic mutations or variants associated with protein S deficiency, allowing for more personalized treatment and management plans.
  6. Family planning: NGS can identify genetic mutations in Pros1 gene protein S deficiency that can be passed on to future generations. This information can be used for family planning decisions and genetic counseling.

It is important to note that while NGS offers several advantages, it also has limitations, such as the potential for identifying variants of uncertain significance and the need for additional confirmatory testing. Therefore, it is crucial to consult with a genetic counselor or healthcare professional to fully understand the implications of NGS testing and its results.

Test Name: PROS1 Gene Protein S Deficiency autosomal dominant 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 PROS1 Gene Protein S Deficiency, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PROS1 Gene Protein S Deficiency, autosomal dominant NGS Genetic DNA Test gene PROS1

Test Name PROS1 Gene Protein S Deficiency autosomal dominant 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 PROS1 Gene Protein S Deficiency, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PROS1 Gene Protein S Deficiency, autosomal dominant NGS Genetic DNA Test gene PROS1
Test Details

Pros1 gene protein S deficiency is a genetic disorder that affects the production or function of protein S, a protein that plays a critical role in preventing blood clot formation. Autosomal dominant inheritance means that a person only needs to inherit one copy of the defective gene from either parent to develop the condition.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes. When it comes to Pros1 gene protein S deficiency, NGS genetic testing offers several advantages:

1. Comprehensive analysis: NGS can analyze multiple genes simultaneously, providing a comprehensive evaluation of the genetic basis of protein S deficiency. This can help identify other potential genetic factors contributing to the disorder and rule out other related conditions.

2. Cost-effective: NGS allows for the analysis of multiple genes in a single test, making it more cost-effective compared to traditional Sanger sequencing, which analyzes genes one at a time.

3. Time-efficient: NGS can analyze a large number of genes within a relatively short period, providing quicker results compared to traditional sequencing methods.

4. Increased diagnostic yield: NGS has a higher diagnostic yield compared to traditional methods, as it can detect a wider range of genetic variations, including single nucleotide variants, insertions, deletions, and structural rearrangements.

5. Personalized treatment: NGS can help identify specific genetic mutations or variants associated with protein S deficiency, allowing for more personalized treatment and management plans.

6. Family planning: NGS can identify genetic mutations in Pros1 gene protein S deficiency that can be passed on to future generations. This information can be used for family planning decisions and genetic counseling.

It is important to note that while NGS offers several advantages, it also has limitations, such as the potential for identifying variants of uncertain significance and the need for additional confirmatory testing. Therefore, it is crucial to consult with a genetic counselor or healthcare professional to fully understand the implications of NGS testing and its results.

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