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GARS1 Gene Neuronopathy Distal Hereditary Motor Type 5 Genetic Test Cost

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

-21%

The GARS1 Gene Neuronopathy Distal Hereditary Motor Type 5 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the GARS1 gene, which are implicated in the development of Distal Hereditary Motor Neuronopathy Type V (dHMN-V). This condition is a rare genetic disorder characterized by progressive weakness and atrophy of the distal muscles, primarily affecting the limbs. The GARS1 gene plays a crucial role in the development and function of peripheral neurons, and mutations can lead to the disruption of these processes, manifesting in the clinical symptoms of dHMN-V.

The test involves the collection of a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed using advanced genetic sequencing techniques to detect the presence of mutations in the GARS1 gene. It is a vital tool for clinicians in confirming a diagnosis, allowing for a better understanding of the condition, and facilitating informed decisions regarding management and treatment options.

At DNA Labs UAE, the cost of the GARS1 Gene Neuronopathy Distal Hereditary Motor Type 5 Genetic Test is set at 4400 AED. This price reflects the sophisticated nature of the testing process and the specialized expertise required to interpret the results accurately. For patients and families affected by this condition, the test represents a crucial step towards achieving a definitive diagnosis and accessing appropriate care and support.

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GARS1 Gene Neuronopathy distal hereditary motor type 5 Genetic Test

Test Details

GARS1 gene neuronopathy, also known as distal hereditary motor neuropathy type 5 (dHMN-V), is a rare genetic disorder that affects the peripheral nerves, specifically the motor neurons. It is caused by mutations in the GARS1 gene, which encodes an enzyme called glycyl-tRNA synthetase.

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 GARS1 gene neuronopathy, NGS genetic testing can be used to identify mutations in the GARS1 gene that are associated with the condition.

NGS genetic testing for GARS1 gene neuronopathy involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the GARS1 gene and potentially other relevant genes. The sequencing data is then analyzed to identify any mutations or variants that may be causing the disorder.

This type of genetic testing can help confirm a diagnosis of GARS1 gene neuronopathy in individuals with symptoms suggestive of the condition. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families with a known GARS1 gene mutation.

It is important to note that genetic testing for GARS1 gene neuronopathy may not be available in all healthcare settings and may require a referral to a specialized genetic testing laboratory. Genetic counseling is typically recommended both before and after genetic testing to discuss the potential implications of the results and to provide support and guidance to individuals and families.

Test Name: GARS1 Gene Neuronopathy distal hereditary motor type 5 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

  • Neurological Disorders

Doctor

  • Neurologist

Test Department

  • Genetics

Pre Test Information

  • Clinical History of Patient who is going for GARS1 Gene Neuronopathy distal hereditary motor type 5 NGS Genetic DNA Test
  • A Genetic Counselling session to draw a pedigree chart of family members affected with GARS1 Gene Neuronopathy distal hereditary motor type 5
Test Name GARS1 Gene Neuronopathy distal hereditary motor type 5 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 GARS1 Gene Neuronopathy distal hereditary motor type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GARS1 Gene Neuronopathy distal hereditary motor type 5
Test Details

GARS1 gene neuronopathy, also known as distal hereditary motor neuropathy type 5 (dHMN-V), is a rare genetic disorder that affects the peripheral nerves, specifically the motor neurons. It is caused by mutations in the GARS1 gene, which encodes an enzyme called glycyl-tRNA synthetase.

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 GARS1 gene neuronopathy, NGS genetic testing can be used to identify mutations in the GARS1 gene that are associated with the condition.

NGS genetic testing for GARS1 gene neuronopathy involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the GARS1 gene and potentially other relevant genes. The sequencing data is then analyzed to identify any mutations or variants that may be causing the disorder.

This type of genetic testing can help confirm a diagnosis of GARS1 gene neuronopathy in individuals with symptoms suggestive of the condition. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families with a known GARS1 gene mutation.

It is important to note that genetic testing for GARS1 gene neuronopathy may not be available in all healthcare settings and may require a referral to a specialized genetic testing laboratory. Genetic counseling is typically recommended both before and after genetic testing to discuss the potential implications of the results and to provide support and guidance to individuals and families.