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. |
