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SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency Genetic Test Cost

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

-21%

The SLC16A1 gene encodes for Monocarboxylate Transporter 1 (MCT1), a crucial protein involved in the transport of lactate and other monocarboxylates across cell membranes, playing a vital role in cellular metabolism. A deficiency in this transporter, due to mutations in the SLC16A1 gene, can lead to various metabolic disorders, impacting the body’s ability to process and utilize monocarboxylates effectively.

The SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency Genetic Test is a specialized diagnostic tool designed to identify mutations in the SLC16A1 gene that could lead to MCT1 deficiency. This test is particularly important for individuals presenting symptoms of metabolic disorders or for those with a family history of such conditions, as it can provide a definitive diagnosis and guide treatment and management strategies.

Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a comprehensive analysis of the SLC16A1 gene. The cost of the test is set at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic variations associated with MCT1 deficiency. Through this test, patients and healthcare providers can gain crucial insights into the genetic basis of metabolic disorders, enabling personalized treatment plans and potentially improving patient outcomes.

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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.

SKU: TEST-2556 Category:

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