Short Description

NGS genetic DNA test detecets for variant and mutation detection in DOLK gene for Glycosylation disorder type 1M

PreTest 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

Detail Description

DNA Labs India: DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test Cost INR 20,000

DNA Labs India is a leading diagnostic laboratory in India that offers a comprehensive range of genetic testing services. One of the tests offered by the lab is the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test. This test is designed to help diagnose DOLK gene glycosylation disorder type 1M, a rare genetic disorder that affects the glycosylation process in the body.

What is DOLK Gene Glycosylation Disorder Type 1M?

DOLK gene glycosylation disorder type 1M is a rare genetic disorder that affects the glycosylation process in the body. Glycosylation is a process in which sugar molecules are added to proteins and lipids to form glycoproteins and glycolipids, which are important for various cellular functions.

In individuals with DOLK gene glycosylation disorder type 1M, the DOLK gene is mutated, which leads to an impairment in the glycosylation process. This can result in a range of symptoms, including developmental delay, intellectual disability, seizures, hypotonia, and abnormal facial features.

What is the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test?

The DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test is a genetic test that uses next-generation sequencing (NGS) technology to analyze the DOLK gene. This test can help diagnose DOLK gene glycosylation disorder type 1M by detecting mutations in the DOLK gene.

The test requires a small blood sample, which is analyzed in a laboratory using NGS technology. The results of the test can help healthcare professionals diagnose DOLK gene glycosylation disorder type 1M and provide appropriate treatment and management.

What are the Symptoms of DOLK Gene Glycosylation Disorder Type 1M?

The symptoms of DOLK gene glycosylation disorder type 1M can vary from person to person. Some common symptoms include:

• Developmental delay
• Intellectual disability
• Seizures
• Hypotonia (low muscle tone)
• Abnormal facial features

Other symptoms may include feeding difficulties, vision problems, hearing loss, and skeletal abnormalities.

How is DOLK Gene Glycosylation Disorder Type 1M Diagnosed?

DOLK gene glycosylation disorder type 1M is diagnosed through genetic testing, such as the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test. Other diagnostic tests may include blood tests, imaging tests, and developmental assessments.

If you or your child is experiencing symptoms of DOLK gene glycosylation disorder type 1M, it is important to speak with a healthcare professional for an accurate diagnosis.

What is the Cost of the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test?

The cost of the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test at DNA Labs India is INR 20,000. This cost includes the test, sample collection, and analysis.

Conclusion

The DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test offered by DNA Labs India is an important diagnostic tool for individuals experiencing symptoms of DOLK gene glycosylation disorder type 1M. The test is non-invasive, easy to perform, and provides accurate results.

If you or a loved one is experiencing symptoms of DOLK gene glycosylation disorder type 1M, it is important to speak with a healthcare professional for an accurate diagnosis and appropriate treatment.

For more information about the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test or other genetic testing services offered by DNA Labs India, visit their website or contact their customer support team.

Remember, early diagnosis and treatment can make a significant difference in the management of genetic disorders.