FOLR1 Gene Neurodegeneration Due to Cerebral Folate Transport Deficiency Genetic Test sale cost 4400 AED
MEGF10 Gene Myopathy Areflexia Respiratory Distress and Dysphagia Early-Onset Genetic Test sale cost 4400 AED MEGF10 Gene Myopathy Areflexia Respiratory Distress and Dysphagia Early-Onset Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
CNTNAP4 Gene Neurodevelopmental Disorder CNTNAP4 Related Genetic Test sale cost 4400 AED CNTNAP4 Gene Neurodevelopmental Disorder CNTNAP4 Related Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

FOLR1 Gene Neurodegeneration Due to Cerebral Folate Transport Deficiency Genetic Test Cost

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

-21%

The FOLR1 gene plays a crucial role in the transportation of folate across the blood-brain barrier, a vital process for normal neurological development and function. Mutations in the FOLR1 gene can lead to cerebral folate transport deficiency, a condition characterized by a spectrum of neurological symptoms ranging from developmental delays to severe neurodegeneration. Early detection and diagnosis through genetic testing can be pivotal in managing symptoms and improving the quality of life for affected individuals.

DNA Labs UAE offers a comprehensive genetic test for detecting mutations in the FOLR1 gene, which is essential for diagnosing cerebral folate transport deficiency. The test, priced at 4400 AED, involves analyzing the patient’s DNA to identify any alterations in the FOLR1 gene that might impede the normal transport of folate into the brain. This precise genetic testing provides invaluable insights for clinicians to devise appropriate treatment strategies, potentially involving folinic acid supplementation to mitigate the effects of reduced folate transport.

By availing of this test at DNA Labs UAE, individuals suspected of having cerebral folate transport deficiency can receive a definitive diagnosis, enabling timely and targeted interventions. This not only aids in alleviating symptoms but also significantly contributes to preventing the progression of neurodegeneration associated with this condition.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

FOLR1 Gene Neurodegeneration due to cerebral folate transport deficiency Genetic Test

Welcome to DNA Labs UAE, where we offer the FOLR1 Gene Neurodegeneration due to cerebral folate transport deficiency Genetic Test. This test is designed to diagnose and provide information about the condition known as neurodegeneration due to cerebral folate transport deficiency (NCFTD).

Test Details

The FOLR1 gene is associated with NCFTD, a condition characterized by the brain’s inability to transport folate (vitamin B9) into the cerebral spinal fluid. This leads to a deficiency of folate in the brain, resulting in neurodegeneration.

Our NGS (Next-Generation Sequencing) technology allows us to analyze the DNA sequence of an individual’s genes. This enables us to detect genetic variations, such as mutations or variants, that may be associated with NCFTD.

Test Components and Price

  • Test Name: FOLR1 Gene Neurodegeneration due to cerebral folate transport deficiency Genetic Test
  • Price: 4400.0 AED

Sample Condition

We require either blood, extracted DNA, or one drop of blood on an FTA card as the sample condition for this test.

Report Delivery

The report will be delivered within 3 to 4 weeks after the test.

Test Type

This test falls under the category of Neurological Disorders.

Referring Doctor and Test Department

Our referring doctor for this test is a Neurologist, and the test is conducted in our Genetics department.

Pre Test Information

Prior to the test, we recommend providing the clinical history of the patient who is going for the FOLR1 Gene Neurodegeneration due to cerebral folate transport deficiency NGS Genetic DNA Test. Additionally, a Genetic Counselling session is conducted to draw a pedigree chart of family members affected with NCFTD.

Importance of NGS Genetic Testing

NGS genetic testing is crucial in identifying mutations or variants in the FOLR1 gene that may be causing neurodegeneration due to cerebral folate transport deficiency. This not only helps in confirming a diagnosis but also aids in determining appropriate treatment options for affected individuals.

It is essential to note that NGS genetic testing should always be conducted by a qualified healthcare professional or genetic counselor. These experts can interpret the results and provide appropriate guidance and support throughout the process.

Test Name FOLR1 Gene Neurodegeneration due to cerebral folate transport deficiency 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 FOLR1 Gene Neurodegeneration due to cerebral folate transport deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FOLR1 Gene Neurodegeneration due to cerebral folate transport deficiency
Test Details

The FOLR1 gene is associated with a condition called neurodegeneration due to cerebral folate transport deficiency (NCFTD). This condition is characterized by the inability of the brain to transport folate (vitamin B9) into the cerebral spinal fluid, leading to a deficiency of folate in the brain.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of genetic variations, such as mutations or variants, that may be associated with certain diseases or conditions.

In the case of neurodegeneration due to cerebral folate transport deficiency, NGS genetic testing can be used to identify mutations or variants in the FOLR1 gene that may be causing the condition. This can help in confirming a diagnosis and determining the appropriate treatment options for individuals with this condition.

It is important to note that NGS genetic testing should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

SKU: TEST-1827 Category:

Related products