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MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test Cost

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

-21%

The MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test is a specialized diagnostic tool used to identify mutations in the MPDU1 gene, which can lead to a rare condition known as Congenital Disorder of Glycosylation Type 1F (CDG-1F). CDG-1F is a genetic disorder that affects the normal process of glycosylation, an essential biological mechanism where sugar molecules are attached to proteins and lipids, impacting various bodily functions.

This specific test targets the MPDU1 gene to detect abnormalities that disrupt normal glycosylation processes, leading to a range of symptoms such as developmental delay, neurological issues, and abnormalities in liver function among others. Given the complexity and rarity of the condition, the test provides crucial information for accurate diagnosis, which is vital for managing symptoms and improving the quality of life for affected individuals.

The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test is 4400 AED. This price reflects the sophisticated nature of the testing process, which involves advanced genetic sequencing techniques to accurately identify mutations in the MPDU1 gene. By opting for this test at DNA Labs UAE, patients and healthcare providers can expect reliable results, which are essential for the effective management and treatment of CDG-1F.

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MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test

Welcome to DNA Labs UAE, where we offer comprehensive genetic testing services. In this blog, we will discuss the MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test, including its cost, symptoms, diagnosis, and other relevant information.

Test Name: MPDU1 Gene Glycosylation Disorder Type 1F 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 MPDU1 Gene Glycosylation Disorder Type 1F NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Glycosylation Disorder Type 1F.

Test Details:

The MPDU1 gene is responsible for encoding the enzyme mannosyl-oligosaccharide glucosidase, which is involved in the glycosylation process. Glycosylation disorders, such as type 1F, result from mutations in the MPDU1 gene, leading to impaired glycosylation of proteins.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of MPDU1 gene glycosylation disorder type 1F, NGS genetic testing can be used to identify mutations or variants in the MPDU1 gene that may be causing the glycosylation disorder.

This type of genetic testing can provide valuable information for diagnosis, prognosis, and potential treatment options for individuals with MPDU1 gene glycosylation disorder type 1F. It can also help in identifying carriers of the mutation and provide information for family planning and genetic counseling.

Test Name MPDU1 Gene Glycosylation disorder type 1F 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 MPDU1 Gene Glycosylation disorder type 1F NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glycosylation disorder type 1F
Test Details

The MPDU1 gene is responsible for encoding the enzyme mannosyl-oligosaccharide glucosidase, which is involved in the glycosylation process. Glycosylation disorders, such as type 1F, result from mutations in the MPDU1 gene, leading to impaired glycosylation of proteins.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of MPDU1 gene glycosylation disorder type 1F, NGS genetic testing can be used to identify mutations or variants in the MPDU1 gene that may be causing the glycosylation disorder.

This type of genetic testing can provide valuable information for diagnosis, prognosis, and potential treatment options for individuals with MPDU1 gene glycosylation disorder type 1F. It can also help in identifying carriers of the mutation and provide information for family planning and genetic counseling.