SLC16A1 Gene Monocarboxylate transporter 1 deficiency Genetic Test
At DNA Labs UAE, we offer the SLC16A1 Gene Monocarboxylate transporter 1 deficiency Genetic Test at a cost of AED 4400.0.
Test Details
The SLC16A1 gene monocarboxylate transporter 1 deficiency is a genetic disorder that affects the transportation of monocarboxylates, such as lactate and pyruvate, across cell membranes. This deficiency can lead to various symptoms and health problems, including developmental delay, intellectual disability, epilepsy, muscle weakness, and metabolic abnormalities.
Our genetic testing method utilizes NGS (Next-Generation Sequencing) technology, which allows for the analysis of multiple genes simultaneously. In the case of SLC16A1 gene monocarboxylate transporter 1 deficiency, NGS genetic testing can identify mutations or variants in the SLC16A1 gene that may be causing the disorder.
NGS genetic testing provides valuable information about an individual’s genetic makeup and helps in diagnosing genetic disorders. It can also be used for carrier testing, prenatal testing, and predicting the risk of certain genetic conditions. The results of NGS genetic testing can guide medical management and treatment decisions for individuals with SLC16A1 gene monocarboxylate transporter 1 deficiency.
Test Components and Price
- Test Name: SLC16A1 Gene Monocarboxylate transporter 1 deficiency Genetic Test
- Components: Blood or Extracted DNA or One drop Blood on FTA Card
- Price: AED 4400.0
Report Delivery
The report will be delivered within 3 to 4 weeks after the sample is received.
Test Type and Department
- Test Type: Metabolic Disorders
- Test Department: Genetics
Referring Doctor
The referring doctor for this test is a General Physician.
Pre Test Information
Prior to the SLC16A1 Gene Monocarboxylate transporter 1 deficiency NGS Genetic DNA Test, a clinical history of the patient is required. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with Monocarboxylate transporter 1 deficiency.
| Test Name | SLC16A1 Gene Monocarboxylate transporter 1 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 SLC16A1 Gene Monocarboxylate transporter 1 deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Monocarboxylate transporter 1 deficiency |
| Test Details |
SLC16A1 gene monocarboxylate transporter 1 deficiency is a genetic disorder that affects the transportation of monocarboxylates, such as lactate and pyruvate, across cell membranes. This deficiency can lead to various symptoms and health problems, including developmental delay, intellectual disability, epilepsy, muscle weakness, and metabolic abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of SLC16A1 gene monocarboxylate transporter 1 deficiency, NGS genetic testing can be used to identify mutations or variants in the SLC16A1 gene that may be causing the disorder. NGS genetic testing can provide valuable information about an individual’s genetic makeup and help in diagnosing genetic disorders. It can also be used for carrier testing, prenatal testing, and predicting the risk of certain genetic conditions. The results of NGS genetic testing can guide medical management and treatment decisions for individuals with SLC16A1 gene monocarboxylate transporter 1 deficiency. |
