ALG6 Gene Glycosylation Disorder Type 1C Genetic Test
Welcome to DNA Labs UAE, where we offer the ALG6 Gene Glycosylation Disorder Type 1C Genetic Test. This test is designed to detect mutations in the ALG6 gene that may cause glycosylation disorder type 1C.
Test Details
The ALG6 gene glycosylation disorder type 1C NGS genetic test is a diagnostic test that analyzes the DNA sequence of the ALG6 gene. By identifying mutations in this gene, we can detect the deficiency in the enzyme ALG6, which is responsible for adding sugar molecules to proteins and lipids in the body.
Individuals with glycosylation disorder type 1C may experience a range of symptoms, including developmental delays, intellectual disability, seizures, and abnormal facial features. Early diagnosis and management of the disorder is crucial for effective treatment.
Our NGS genetic test utilizes next-generation sequencing technology to identify mutations in the ALG6 gene. This advanced technology allows for accurate and reliable results, providing valuable information for healthcare professionals and patients.
Test Components and Price
The ALG6 Gene Glycosylation Disorder Type 1C Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card. The report delivery time is approximately 3 to 4 weeks.
Test Type and Doctor
The ALG6 Gene Glycosylation Disorder Type 1C Genetic Test falls under the category of neurological disorders. It is recommended to consult with a neurologist for this test.
Test Department and Pre Test Information
This test is conducted in our Genetics department. Before undergoing the ALG6 Gene Glycosylation Disorder Type 1C Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by ALG6 Gene Glycosylation Disorder Type 1C.
| Test Name | ALG6 Gene Glycosylation disorder type 1C 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 ALG6 Gene Glycosylation disorder type 1C NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ALG6 Gene Glycosylation disorder type 1C |
| Test Details |
ALG6 gene glycosylation disorder type 1C NGS genetic test is a diagnostic test that analyzes the DNA sequence of the ALG6 gene to detect mutations that may cause glycosylation disorder type 1C. This disorder is caused by a deficiency in the enzyme ALG6, which is responsible for adding sugar molecules to proteins and lipids in the body. This deficiency results in abnormal glycosylation of these molecules, leading to a range of symptoms such as developmental delays, intellectual disability, seizures, and abnormal facial features. The NGS genetic test uses next-generation sequencing technology to identify mutations in the ALG6 gene, allowing for early diagnosis and management of the disorder. |
