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NR2E1 Gene Polymicrogyria Bilateral Occipital Genetic Test Cost

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

-21%

The NR2E1 gene plays a significant role in brain development, and mutations in this gene are linked to a rare neurological condition known as polymicrogyria, specifically affecting the occipital lobes bilaterally. Polymicrogyria is characterized by an excessive number of small and malformed cerebral cortical folds, which can lead to a range of neurological issues, including developmental delays, seizures, and difficulties with coordination and speech.

To diagnose this genetic condition, DNA Labs UAE offers a specialized genetic test targeting the NR2E1 gene. This test is designed to identify mutations that may be responsible for bilateral occipital polymicrogyria, providing crucial information for accurate diagnosis and potential management strategies for affected individuals. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately detect and interpret mutations in the NR2E1 gene. Conducting this test can be a critical step for families seeking answers to developmental and neurological challenges faced by their loved ones, enabling access to targeted support and interventions.

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NR2E1 Gene Polymicrogyria bilateral occipital Genetic Test

Test Name: NR2E1 Gene Polymicrogyria bilateral occipital 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 NR2E1 Gene Polymicrogyria bilateral occipital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NR2E1 Gene Polymicrogyria bilateral occipital.

Test Details

The NR2E1 gene is associated with a condition called Polymicrogyria, which is a type of brain malformation characterized by an excessive number of small folds (gyri) in the cerebral cortex. Bilateral occipital polymicrogyria specifically refers to the presence of these abnormal folds in the occipital lobes of both sides of the brain.

NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic test that uses advanced sequencing technologies to rapidly and accurately analyze multiple genes simultaneously. In the context of Polymicrogyria, NGS Genetic Testing can be used to identify any mutations or variations in the NR2E1 gene that may be responsible for the condition.

By analyzing the DNA sequence of the NR2E1 gene, NGS Genetic Testing can help diagnose Polymicrogyria and provide valuable information about the genetic cause of the condition. This can aid in understanding the inheritance pattern, providing genetic counseling, and potentially guiding treatment decisions.

Test Name NR2E1 Gene Polymicrogyria bilateral occipital 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 NR2E1 Gene Polymicrogyria bilateral occipital NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NR2E1 Gene Polymicrogyria bilateral occipital
Test Details

The NR2E1 gene is associated with a condition called Polymicrogyria, which is a type of brain malformation characterized by an excessive number of small folds (gyri) in the cerebral cortex. Bilateral occipital polymicrogyria specifically refers to the presence of these abnormal folds in the occipital lobes of both sides of the brain.

NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic test that uses advanced sequencing technologies to rapidly and accurately analyze multiple genes simultaneously. In the context of Polymicrogyria, NGS Genetic Testing can be used to identify any mutations or variations in the NR2E1 gene that may be responsible for the condition.

By analyzing the DNA sequence of the NR2E1 gene, NGS Genetic Testing can help diagnose Polymicrogyria and provide valuable information about the genetic cause of the condition. This can aid in understanding the inheritance pattern, providing genetic counseling, and potentially guiding treatment decisions.

SKU: TEST-1919 Category:

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