Sale!

DOLK Gene Glycosylation Disorder Type 1M Genetic Test

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

-21%

The DOLK Gene Glycosylation Disorder Type 1M Genetic Test is a specialized diagnostic assessment designed to identify mutations in the DOLK gene, which can lead to Congenital Disorders of Glycosylation Type 1m (CDG-1m). This condition is a rare genetic disorder that affects the normal process of glycosylation, the attachment of sugars to proteins and lipids, which is crucial for various cellular functions. Mutations in the DOLK gene disrupt this process, leading to a range of symptoms including developmental delay, skin abnormalities, and potential issues with the heart, liver, and muscles.

The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. Utilizing advanced genetic sequencing technologies, the test examines the DOLK gene for specific mutations known to cause the disorder. This precise approach allows for an accurate diagnosis, which is essential for developing an effective treatment plan and providing genetic counseling.

The cost of the DOLK Gene Glycosylation Disorder Type 1M Genetic Test is 4400 AED. While the price may seem significant, the value of obtaining a precise diagnosis cannot be overstated, as it opens the door to targeted interventions that can significantly improve the quality of life for affected individuals. Additionally, the test provides vital information for family planning and the assessment of risk for future children.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

DOLK Gene Glycosylation Disorder Type 1M Genetic Test

Test Details

DOLK gene glycosylation disorder type 1M is a rare genetic disorder that affects the process of glycosylation, which is the attachment of sugar molecules to proteins and lipids. This disorder is caused by mutations in the DOLK gene, which provides instructions for making an enzyme that is necessary for the proper glycosylation of proteins.

Test Name

DOLK Gene Glycosylation Disorder Type 1M 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

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DOLK Gene Glycosylation Disorder Type 1M.

Introduction to NGS Genetic Testing

NGS genetic testing, also known as next-generation sequencing, is a type of genetic testing that can analyze multiple genes at once to identify mutations or variants that may be responsible for a genetic disorder. This type of testing can be useful for diagnosing rare genetic disorders like DOLK gene glycosylation disorder type 1M.

NGS genetic testing involves sequencing the DNA of the patient using high-throughput sequencing technology, which allows for the analysis of millions of DNA sequences at once. The results of the test can then be compared to a reference genome to identify any mutations or variants that may be associated with the disorder.

Benefits of NGS Genetic Testing for DOLK Gene Glycosylation Disorder Type 1M

NGS genetic testing for DOLK gene glycosylation disorder type 1M can help with early diagnosis and treatment of the disorder, as well as provide information for genetic counseling and family planning. However, it is important to note that genetic testing is not a replacement for clinical evaluation and diagnosis by a healthcare professional.

Test Name DOLK Gene Glycosylation disorder type 1M Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for DOLK Gene Glycosylation disorder type 1M NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DOLK Gene Glycosylation disorder type 1M
Test Details

DOLK gene glycosylation disorder type 1M is a rare genetic disorder that affects the process of glycosylation, which is the attachment of sugar molecules to proteins and lipids. This disorder is caused by mutations in the DOLK gene, which provides instructions for making an enzyme that is necessary for the proper glycosylation of proteins.

NGS genetic testing, also known as next-generation sequencing, is a type of genetic testing that can analyze multiple genes at once to identify mutations or variants that may be responsible for a genetic disorder. This type of testing can be useful for diagnosing rare genetic disorders like DOLK gene glycosylation disorder type 1M.

NGS genetic testing involves sequencing the DNA of the patient using high-throughput sequencing technology, which allows for the analysis of millions of DNA sequences at once. The results of the test can then be compared to a reference genome to identify any mutations or variants that may be associated with the disorder.

NGS genetic testing for DOLK gene glycosylation disorder type 1M can help with early diagnosis and treatment of the disorder, as well as provide information for genetic counseling and family planning. However, it is important to note that genetic testing is not a replacement for clinical evaluation and diagnosis by a healthcare professional.