SLC2A2 Gene Fanconi-Bickel Syndrome Genetic Test
Welcome to DNA Labs UAE, where we offer the SLC2A2 Gene Fanconi-Bickel Syndrome Genetic Test at a cost of AED 4400.0.
Test Details
The SLC2A2 gene is responsible for encoding the glucose transporter 2 protein, which plays a crucial role in transporting glucose into cells. Mutations in this gene can lead to a rare genetic disorder called Fanconi-Bickel syndrome.
Fanconi-Bickel syndrome is an autosomal recessive disorder characterized by impaired glucose transport and metabolism. This results in the accumulation of glucose in the blood and the inability of cells to utilize glucose for energy production.
Symptoms of this condition include hepatomegaly (enlarged liver), growth retardation, renal dysfunction, and rickets.
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
Prior to undergoing the SLC2A2 Gene Fanconi-Bickel Syndrome NGS Genetic DNA Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with Fanconi-Bickel syndrome.
NGS Technology
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the SLC2A2 gene. This test can identify mutations or variants in the SLC2A2 gene that may be responsible for Fanconi-Bickel syndrome.
NGS testing is a powerful tool for diagnosing genetic disorders, as it can detect both common and rare mutations in multiple genes at once.
Consultation and Interpretation
If you suspect that you or your child may have Fanconi-Bickel syndrome, it is recommended to consult with a genetic counselor or healthcare provider. They can guide you through the testing process and help interpret the results.
| Test Name | SLC2A2 Gene Fanconi-Bickel 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for SLC2A2 Gene Fanconi-Bickel syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi-Bickel syndrome |
| Test Details |
The SLC2A2 gene is responsible for encoding the glucose transporter 2 protein, which plays a crucial role in transporting glucose into cells. Mutations in this gene can lead to a rare genetic disorder called Fanconi-Bickel syndrome. Fanconi-Bickel syndrome is an autosomal recessive disorder characterized by impaired glucose transport and metabolism. This results in the accumulation of glucose in the blood and the inability of cells to utilize glucose for energy production. Symptoms of this condition include hepatomegaly (enlarged liver), growth retardation, renal dysfunction, and rickets. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the SLC2A2 gene. This test can identify mutations or variants in the SLC2A2 gene that may be responsible for Fanconi-Bickel syndrome. NGS testing is a powerful tool for diagnosing genetic disorders, as it can detect both common and rare mutations in multiple genes at once. If you suspect that you or your child may have Fanconi-Bickel syndrome, consulting with a genetic counselor or a healthcare provider is recommended. They can guide you through the testing process and help interpret the results. |
