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OCLN Gene Band-Like Calcification with Simplified Gyration and Polymicrogyria Genetic Test Cost

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

-21%

The “OCLN Gene Band-Like Calcification with Simplified Gyration and Polymicrogyria Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the OCLN gene. These mutations are associated with a rare neurological disorder characterized by band-like calcifications in the brain, simplified gyration, and polymicrogyria, a condition where the brain has many small and irregular folds. This condition can lead to a variety of neurological symptoms and developmental delays. The test involves analyzing the patient’s DNA to identify any genetic alterations in the OCLN gene that could lead to this disorder. The cost of the test is 4400 AED, making it a valuable tool for families seeking answers to complex neurological conditions. By providing a definitive genetic diagnosis, this test can help guide treatment decisions and support services for affected individuals.

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OCLN Gene Band-like Calcification with Simplified Gyration and Polymicrogyria Genetic Test

Are you looking for a genetic test for OCLN Gene Band-like Calcification with Simplified Gyration and Polymicrogyria? DNA Labs UAE offers a comprehensive genetic testing service that can provide you with valuable insights into this rare genetic disorder.

Test Details

The OCLN gene, also known as the occludin gene, is associated with a condition called band-like calcification with simplified gyration and polymicrogyria (BLC-PMG). This rare genetic disorder is characterized by abnormal brain development.

Our genetic testing service utilizes next-generation sequencing (NGS) technology to analyze the OCLN gene for any mutations or variations that may be causing BLC-PMG. By sequencing the OCLN gene, NGS testing can identify specific genetic changes that may be responsible for the condition.

NGS genetic testing is not only useful for diagnostic purposes but also for genetic counseling and family planning. It can help determine the mode of inheritance of BLC-PMG within a family, assess the risk of recurrence in future pregnancies, and guide reproductive decision-making.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics, as the results can have significant implications for individuals and their families.

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

Prior to undergoing the OCLN Gene Band-like Calcification with Simplified Gyration and Polymicrogyria Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with the condition.

This genetic test focuses on the OCLN gene and is specifically designed for individuals suspected of having BLC-PMG.

For accurate and reliable results, it is essential to have the test performed and interpreted by healthcare professionals with expertise in genetics.

Test Name OCLN Gene Band-like calcification with simplified gyration and polymicrogyria 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 OCLN Gene Band-like calcification with simplified gyration and polymicrogyria NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with OCLN Gene Band-like calcification with simplified gyration and polymicrogyria NGS Genetic DNA Test gene OCLN
Test Details

The OCLN gene, also known as the occludin gene, is associated with a condition called band-like calcification with simplified gyration and polymicrogyria (BLC-PMG). BLC-PMG is a rare genetic disorder characterized by abnormal brain development.

NGS genetic testing refers to next-generation sequencing, a high-throughput DNA sequencing technology. In the context of BLC-PMG, NGS genetic testing can be used to analyze the OCLN gene for any mutations or variations that may be causing the condition.

By sequencing the OCLN gene, NGS testing can identify specific genetic changes that may be responsible for BLC-PMG. This information can be used for diagnostic purposes, providing a definitive genetic diagnosis for individuals with suspected BLC-PMG.

NGS genetic testing can also be valuable for genetic counseling and family planning. It can help determine the mode of inheritance of BLC-PMG within a family, assess the risk of recurrence in future pregnancies, and guide reproductive decision-making.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics, as the results can have significant implications for individuals and their families.

SKU: TEST-3996 Category:

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