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ORC4 Gene Meier-Gorlin Syndrome Type 2 Genetic Test Cost

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

-21%

The ORC4 Gene Meier-Gorlin Syndrome Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the ORC4 gene, which are associated with Meier-Gorlin Syndrome Type 2 (MGORS2). Meier-Gorlin Syndrome is a rare genetic disorder characterized by short stature, small ears, and, in some cases, skeletal abnormalities. The ORC4 gene plays a critical role in DNA replication, and mutations in this gene can lead to the developmental issues observed in MGORS2.

The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities in the ORC4 gene. This genetic testing is crucial for accurate diagnosis, allowing for tailored treatment and management plans for affected individuals. It also provides essential information for family planning and genetic counseling for families with a history of the condition.

The cost of the ORC4 Gene Meier-Gorlin Syndrome Type 2 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test, including the expertise required to accurately identify and interpret mutations in the ORC4 gene. Families and individuals considering this test are encouraged to discuss it with their healthcare provider to understand its benefits and implications fully.

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ORC4 Gene Meier-Gorlin Syndrome Type 2 Genetic Test

At DNA Labs UAE, we offer the ORC4 Gene Meier-Gorlin Syndrome Type 2 Genetic Test. This test is designed to diagnose Meier-Gorlin Syndrome Type 2, a rare genetic disorder characterized by short stature, small ears, and skeletal abnormalities.

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

Before undergoing the ORC4 Gene Meier-Gorlin Syndrome Type 2 Genetic Test, it is important 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 by Meier-Gorlin Syndrome Type 2 and the ORC4 gene.

Test Details

The ORC4 gene is associated with Meier-Gorlin Syndrome Type 2. Our NGS (Next-Generation Sequencing) genetic testing method allows us to analyze multiple genes simultaneously, including the ORC4 gene, to identify any genetic variations or mutations that may be responsible for the disorder.

This test can help confirm a diagnosis, provide information about disease severity and progression, and guide treatment options and management strategies. It is crucial to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of genetic testing for Meier-Gorlin Syndrome Type 2. They can also help you understand the potential benefits, limitations, and implications of the test results.

Test Name ORC4 Gene Meier-Gorlin syndrome type 2 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 ORC4 Gene Meier-Gorlin syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ORC4 Gene Meier-Gorlin syndrome type 2 NGS Genetic DNA Test gene ORC4
Test Details

The ORC4 gene is associated with Meier-Gorlin syndrome type 2, a rare genetic disorder characterized by short stature, small ears, and skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be responsible for a particular condition.

An NGS genetic test for Meier-Gorlin syndrome type 2 would involve sequencing the ORC4 gene and potentially other related genes to look for any genetic variations or mutations that may be causing the disorder. This test can help confirm a diagnosis, provide information about disease severity and progression, and guide treatment options and management strategies.

It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of genetic testing for Meier-Gorlin syndrome type 2 and to understand the potential benefits, limitations, and implications of the test results.