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GTPBP2 Gene Neurodegeneration with Brain Iron Accumulation GTPBP2 Related Genetic Test

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

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The GTPBP2 gene plays a significant role in the neurological disorder known as Neurodegeneration with Brain Iron Accumulation (NBIA). NBIA is characterized by the accumulation of iron in the brain, particularly in the basal ganglia, leading to a range of movement disorders and neurodegenerative symptoms. Mutations in the GTPBP2 gene have been identified as one of the genetic causes behind certain forms of this disorder. These mutations can disrupt normal cellular functions, leading to the progressive degeneration of nervous tissue and the hallmark iron accumulation.

To diagnose and understand the specific genetic underpinnings of NBIA in patients suspected of having GTPBP2-related neurodegeneration, genetic testing is essential. DNA Labs UAE offers a comprehensive genetic test targeting the GTPBP2 gene to identify mutations that may be responsible for the condition. The test is crucial for accurate diagnosis, which can guide treatment decisions and genetic counseling.

The cost of the GTPBP2-related genetic test at DNA Labs UAE is 4400 AED. This investment covers the meticulous process of DNA analysis to detect the presence of mutations in the GTPBP2 gene. By opting for this test, patients and their families can gain valuable insights into the genetic basis of their condition, opening the door to targeted therapies and interventions that can improve quality of life and manage symptoms more effectively.

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GTPBP2 Gene Neurodegeneration with brain iron accumulation – Genetic Test

At DNA Labs UAE, we offer a comprehensive genetic test for GTPBP2 Gene Neurodegeneration with brain iron accumulation. This test can help diagnose and provide valuable information for individuals affected by this condition.

Test Name: GTPBP2 Gene Neurodegeneration with brain iron accumulation GTPBP2 related Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information

Prior to the genetic test, it is important to provide the clinical history of the patient who is going for GTPBP2 Gene Neurodegeneration with brain iron accumulation test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with GTPBP2 Gene Neurodegeneration with brain iron accumulation.

Test Details

Neurodegeneration with brain iron accumulation (NBIA) is a group of inherited neurodegenerative disorders characterized by the abnormal accumulation of iron in the brain. One of the genes associated with NBIA is the GTPBP2 gene. The GTPBP2 gene provides instructions for making a protein called GTP-binding protein 2. This protein is involved in several cellular processes, including the regulation of iron metabolism.

Mutations in the GTPBP2 gene can disrupt the normal function of the protein, leading to the accumulation of iron in the brain and subsequent neurodegeneration. Our genetic test using next-generation sequencing (NGS) technology can identify mutations in the GTPBP2 gene. This involves sequencing the DNA of an individual to look for changes or variations in the gene that may be associated with NBIA.

NGS allows for the simultaneous analysis of multiple genes, making it an efficient method for genetic testing. Identifying mutations in the GTPBP2 gene through NGS can help confirm a diagnosis of NBIA and provide valuable information for genetic counseling and family planning. It can also aid in the development of targeted therapies or interventions for individuals with GTPBP2-related NBIA.

Test Name GTPBP2 Gene Neurodegeneration with brain iron accumulation GTPBP2 related 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 GTPBP2 Gene Neurodegeneration with brain iron accumulation, GTPBP2 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GTPBP2 Gene Neurodegeneration with brain iron accumulation, GTPBP2 related
Test Details

Neurodegeneration with brain iron accumulation (NBIA) is a group of inherited neurodegenerative disorders characterized by the abnormal accumulation of iron in the brain. One of the genes associated with NBIA is the GTPBP2 gene.

The GTPBP2 gene provides instructions for making a protein called GTP-binding protein 2. This protein is involved in several cellular processes, including the regulation of iron metabolism. Mutations in the GTPBP2 gene can disrupt the normal function of the protein, leading to the accumulation of iron in the brain and subsequent neurodegeneration.

A genetic test using next-generation sequencing (NGS) can be performed to identify mutations in the GTPBP2 gene. This test involves sequencing the DNA of an individual to look for changes or variations in the gene that may be associated with NBIA. NGS allows for the simultaneous analysis of multiple genes, making it an efficient method for genetic testing.

Identifying mutations in the GTPBP2 gene through NGS can help confirm a diagnosis of NBIA and provide valuable information for genetic counseling and family planning. It can also aid in the development of targeted therapies or interventions for individuals with GTPBP2-related NBIA.

SKU: TEST-1831 Category:

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