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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 Polymicrogyria Bilateral Occipital Genetic Test is a specialized diagnostic tool used to identify mutations in the NR2E1 gene, which have been associated with bilateral occipital polymicrogyria, a rare neurological condition. This condition is characterized by an excessive number of small and irregularly formed gyri in the occipital lobes of the brain, which can lead to a range of neurological symptoms, including developmental delays, seizures, and visual impairments.

The test involves analyzing the patient’s DNA to detect any genetic variations in the NR2E1 gene that may be indicative of this condition. It is a crucial step for families seeking answers to developmental and neurological issues in their loved ones, as a positive identification of a mutation can guide treatment plans, inform about prognosis, and offer insights into the risk of recurrence in future pregnancies.

Performed at DNA Labs UAE, a leading facility in genetic testing and analysis, the test ensures high accuracy and reliability. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify and interpret genetic mutations associated with bilateral occipital polymicrogyria. Families and individuals undergoing this test at DNA Labs UAE can expect comprehensive support, from pre-test counseling to understand the implications of the test results, to post-test guidance to navigate the next steps in managing the condition.

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NR2E1 Gene Polymicrogyria bilateral occipital Genetic Test

At DNA Labs UAE, we offer the NR2E1 Gene Polymicrogyria bilateral occipital Genetic Test to help diagnose and understand this genetic condition. This test is specifically designed for individuals who are suspected to have NR2E1 gene polymicrogyria bilateral occipital.

Test Components

The NR2E1 Gene Polymicrogyria bilateral occipital Genetic Test includes the following 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the NR2E1 Gene Polymicrogyria bilateral occipital Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with NR2E1 Gene Polymicrogyria bilateral occipital NGS Genetic DNA Test gene NR2E1.

Test Details

The NR2E1 gene is responsible for coding a protein called nuclear receptor subfamily 2, group E, member 1. This protein plays a crucial role in gene expression regulation and the development of the brain and nervous system.

Polymicrogyria is a condition characterized by abnormal brain development, particularly in the cerebral cortex. It is characterized by an excessive number of small folds (gyri) in the brain, resulting in a distinctive “bumpy” appearance. Bilateral occipital polymicrogyria specifically refers to the involvement of the occipital lobes located at the back of the brain.

NGS (Next-Generation Sequencing) genetic testing is a state-of-the-art method that allows for the rapid and accurate analysis of multiple genes simultaneously. In the context of NR2E1 gene polymicrogyria bilateral occipital NGS genetic testing, this test involves sequencing the NR2E1 gene to identify any genetic variations or mutations associated with the condition.

The purpose of this genetic test is to determine if there are any genetic abnormalities in the NR2E1 gene that may contribute to the development of polymicrogyria in the occipital lobes. This information can aid in the diagnosis, prognosis, and potential treatment options for individuals with this condition.

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
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
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 NGS Genetic DNA Test gene NR2E1
Test Details

The NR2E1 gene is a gene that codes for a protein called nuclear receptor subfamily 2, group E, member 1. This protein is involved in the regulation of gene expression and plays a role in the development of the brain and nervous system.

Polymicrogyria is a condition characterized by abnormal brain development, specifically in the cerebral cortex. It is characterized by an excessive number of small folds (gyri) in the brain, leading to a characteristic “bumpy” appearance. Bilateral occipital polymicrogyria refers to the involvement of the occipital lobes, which are located at the back of the brain.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly and accurately analyze multiple genes simultaneously. In the context of NR2E1 gene polymicrogyria bilateral occipital NGS genetic testing, this test would involve sequencing the NR2E1 gene to identify any genetic variations or mutations that may be associated with the condition.

The purpose of this genetic test would be to determine if there are any genetic abnormalities in the NR2E1 gene that may be contributing to the development of polymicrogyria in the occipital lobes. This information can help with diagnosis, prognosis, and potentially guide treatment options for individuals with this condition.

SKU: TEST-4320 Category:

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