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SLC2A1 Gene GLUT1 Deficiency Syndrome Type 1 Genetic Test

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

-21%

The SLC2A1 gene is crucial for encoding the glucose transporter protein GLUT1, which facilitates the transport of glucose across the blood-brain barrier to fuel the brain. GLUT1 Deficiency Syndrome Type 1 is a rare genetic disorder that arises from mutations in the SLC2A1 gene, leading to inadequate glucose transport into the brain. This condition can result in a spectrum of neurological issues, including developmental delay, seizures, movement disorders, and speech difficulties.

To diagnose this condition, a genetic test targeting the SLC2A1 gene can be conducted. This test identifies mutations in the SLC2A1 gene that are responsible for GLUT1 Deficiency Syndrome Type 1. DNA Labs UAE offers this specialized genetic test, providing a crucial tool for diagnosing affected individuals. The test is priced at 4400 AED and involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the SLC2A1 gene.

Early diagnosis through genetic testing is vital for managing GLUT1 Deficiency Syndrome Type 1, as it can guide treatment strategies, including dietary modifications like the ketogenic diet, which has been shown to improve symptoms in affected individuals.

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SLC2A1 Gene GLUT1 Deficiency Syndrome Type 1 Genetic Test

Test Name: SLC2A1 Gene GLUT1 Deficiency Syndrome Type 1 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for SLC2A1 Gene GLUT1 Deficiency Syndrome Type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC2A1 Gene GLUT1 Deficiency Syndrome Type 1.

Test Details

The SLC2A1 gene encodes the glucose transporter type 1 (GLUT1) protein, which is responsible for transporting glucose across the blood-brain barrier. Mutations in this gene can cause GLUT1 deficiency syndrome type 1, a rare genetic disorder characterized by impaired glucose transport to the brain.

NGS (Next-generation sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It can be used to identify mutations in the SLC2A1 gene associated with GLUT1 deficiency syndrome type 1.

NGS genetic testing is a valuable tool for the diagnosis and management of genetic disorders, including GLUT1 deficiency syndrome type 1. It can provide a faster and more comprehensive analysis of multiple genes than traditional genetic testing methods. NGS genetic testing can also help identify individuals who may benefit from early intervention and treatment.

Test Name SLC2A1 Gene GLUT1 deficiency syndrome type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SLC2A1 Gene GLUT1 deficiency syndrome type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SLC2A1 Gene GLUT1 deficiency syndrome type 1
Test Details

SLC2A1 gene encodes the glucose transporter type 1 (GLUT1) protein, which is responsible for transporting glucose across the blood-brain barrier. Mutations in this gene can cause GLUT1 deficiency syndrome type 1, a rare genetic disorder characterized by impaired glucose transport to the brain.

NGS (Next-generation sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It can be used to identify mutations in the SLC2A1 gene associated with GLUT1 deficiency syndrome type 1.

NGS genetic testing is a valuable tool for the diagnosis and management of genetic disorders, including GLUT1 deficiency syndrome type 1. It can provide a faster and more comprehensive analysis of multiple genes than traditional genetic testing methods. NGS genetic testing can also help identify individuals who may benefit from early intervention and treatment.