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MOGS Gene Glycosylation Disorder Type 2B Genetic Test Cost

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

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The “MOGS Gene Glycosylation Disorder Type 2B Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to detect abnormalities in the MOGS gene, which can lead to Congenital Disorders of Glycosylation Type 2B (CDG2B). CDG2B is a rare genetic condition that affects multiple systems of the body, including the nervous system, immune system, and more, leading to a range of symptoms from mild to severe.

This test specifically looks for mutations in the MOGS gene, which plays a crucial role in the glycosylation process—a process vital for proper protein folding and function. Early diagnosis through genetic testing can be crucial in managing symptoms, preventing complications, and improving the quality of life for those affected by the condition.

At DNA Labs UAE, the test is offered at a cost of 4400 AED. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for the presence of mutations in the MOGS gene. Results from this test can provide essential information for families regarding prognosis, treatment options, and the risk of passing the condition on to future generations.

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MOGS Gene Glycosylation Disorder Type 2B Genetic Test

At DNA Labs UAE, we offer the MOGS Gene Glycosylation Disorder Type 2B Genetic Test to diagnose individuals with this rare genetic disorder. This test helps in understanding the glycosylation process in the body, which is crucial for proper protein and lipid function.

Test Details

The MOGS gene glycosylation disorder type 2B is a rare genetic disorder that affects the glycosylation process in the body. Glycosylation involves the attachment of sugar molecules to proteins and lipids, which is essential for their proper function. Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously and identify any mutations or variations in the MOGS gene that may be responsible for glycosylation disorder type 2B.

Components

  • Test Name: MOGS Gene Glycosylation Disorder Type 2B Genetic Test
  • 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: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the MOGS Gene Glycosylation Disorder Type 2B NGS Genetic DNA 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 by Glycosylation Disorder Type 2B. This information is crucial for accurate diagnosis and treatment planning.

Test Process

The MOGS Gene Glycosylation Disorder Type 2B Genetic Test requires a sample of DNA, which can be obtained through a blood or saliva sample. Our advanced NGS technology will then sequence the DNA to identify any variations or mutations in the MOGS gene. The results of this genetic test can help diagnose individuals with glycosylation disorder type 2B and provide valuable information for their medical management and treatment. It can also be used for carrier testing in individuals with a family history of the disorder.

It is important to note that genetic testing for glycosylation disorder type 2B should be performed by healthcare professionals with expertise in genetics. They can provide counseling and guidance based on the results of the genetic test.

Test Name MOGS Gene Glycosylation disorder type 2B 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MOGS Gene Glycosylation disorder type 2B NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glycosylation disorder type 2B
Test Details

MOGS gene glycosylation disorder type 2B is a rare genetic disorder that affects the glycosylation process in the body. Glycosylation is the attachment of sugar molecules to proteins and lipids, which is important for their proper function.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. It can identify mutations or variations in the MOGS gene that may be responsible for glycosylation disorder type 2B.

The NGS genetic test for MOGS gene glycosylation disorder type 2B involves collecting a sample of DNA, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any variations or mutations in the MOGS gene.

This genetic test can help diagnose individuals with glycosylation disorder type 2B and provide valuable information for their medical management and treatment. It can also be used for carrier testing in individuals with a family history of the disorder.

It’s important to note that genetic testing for glycosylation disorder type 2B is typically performed by healthcare professionals with expertise in genetics. They can provide counseling and guidance based on the results of the genetic test.

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