FBP1 Gene Fructose-16-bisphosphatase deficiency Genetic Test
Are you concerned about Fructose-1,6-bisphosphatase deficiency? DNA Labs UAE offers a comprehensive genetic test to analyze the FBP1 gene for mutations or variations associated with this rare inherited metabolic disorder.
Test Details
The FBP1 gene fructose-1,6-bisphosphatase deficiency NGS genetic test utilizes next-generation sequencing (NGS) technology to identify any mutations or variations in the FBP1 gene. This test is specifically designed for the diagnosis of fructose-1,6-bisphosphatase deficiency, which affects the metabolism of fructose-1,6-bisphosphate, a crucial molecule in glucose breakdown for energy production.
By sequencing the entire FBP1 gene, our NGS genetic test can provide valuable information about the specific genetic changes causing the deficiency. This comprehensive analysis allows for the detection of rare or novel mutations that may not be identified by other testing methods.
Our NGS technology enables the analysis of multiple genes simultaneously, making the test more efficient and cost-effective compared to traditional sequencing methods. The results of the FBP1 gene fructose-1,6-bisphosphatase deficiency NGS genetic test can be used for genetic counseling, family planning, and personalized management of the condition.
Test Components and Price
Test Name: FBP1 Gene Fructose-16-bisphosphatase deficiency Genetic Test
Components: NGS Technology
Price: 4400.0 AED
Sample Condition and Report Delivery
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Test Type and Doctor
Test Type: Metabolic Disorders
Doctor: General Physician
Test Department and Pre Test Information
Test Department: Genetics
Pre Test Information: A Genetic Counselling session to draw a pedigree chart of family members affected with Fructose-1,6-bisphosphatase deficiency
Symptoms and Diagnosis
Fructose-1,6-bisphosphatase deficiency is a rare inherited metabolic disorder that can have various symptoms. These symptoms may include hypoglycemia, seizures, lactic acidosis, and developmental delay. Diagnosis of this condition can be confirmed through genetic testing, such as the FBP1 gene fructose-1,6-bisphosphatase deficiency NGS genetic test offered by DNA Labs UAE.
Treatment and Management
Once diagnosed, treatment options for fructose-1,6-bisphosphatase deficiency may include dietary modifications, enzyme replacement therapy, and symptom management. Genetic counseling and personalized management plans can help individuals and families affected by this condition.
Don’t wait any longer. Get the answers you need with the FBP1 Gene Fructose-16-bisphosphatase deficiency Genetic Test at DNA Labs UAE. Contact us today to schedule an appointment.
| Test Name | FBP1 Gene Fructose-16-bisphosphatase 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for FBP1 Gene Fructose-1,6-bisphosphatase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fructose-1,6-bisphosphatase deficiency |
| Test Details |
FBP1 gene fructose-1,6-bisphosphatase deficiency NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the FBP1 gene for mutations or variations that may be associated with fructose-1,6-bisphosphatase deficiency. Fructose-1,6-bisphosphatase deficiency is a rare inherited metabolic disorder that affects the metabolism of fructose-1,6-bisphosphate, a key molecule in the breakdown of glucose for energy production. Mutations in the FBP1 gene can lead to a deficiency of the fructose-1,6-bisphosphatase enzyme, which is necessary for the proper regulation of glucose metabolism. The NGS genetic test for FBP1 gene fructose-1,6-bisphosphatase deficiency involves sequencing the entire FBP1 gene to identify any mutations or variations that may be present. This can help in the diagnosis of the condition and provide information about the specific genetic changes that are causing the deficiency. NGS technology allows for the analysis of multiple genes simultaneously, making it a more efficient and cost-effective method for genetic testing compared to traditional sequencing methods. It can provide a comprehensive analysis of the FBP1 gene and identify rare or novel mutations that may not be detected by other testing methods. The results of the FBP1 gene fructose-1,6-bisphosphatase deficiency NGS genetic test can be used for genetic counseling, family planning, and personalized management of the condition. Treatment options for fructose-1,6-bisphosphatase deficiency may include dietary modifications, enzyme replacement therapy, and symptom management. |
