NCL Enzyme Panel NGS Genetic Test
Are you or your loved one experiencing symptoms of a lysosomal storage disorder (LSD) known as neuronal ceroid lipofuscinoses (NCL)? DNA Labs UAE offers the NCL Enzyme Panel NGS Genetic DNA Test, a cutting-edge genetic test that can help diagnose and manage this disorder.
Test Details
The NCL Enzyme Panel NGS Genetic DNA Test is a type of genetic test that utilizes next-generation sequencing (NGS) technology to analyze a group of genes associated with NCLs. LSDs are inherited disorders that occur when the body fails to break down certain substances within cells. NCLs specifically affect the nervous system and can lead to progressive neurological decline, seizures, and vision loss.
With the NCL Enzyme Panel NGS Genetic DNA Test, we analyze the DNA of an individual to identify any mutations or changes in the genes associated with NCLs. This comprehensive test can detect mutations in up to 13 genes, including CLN1, CLN2, CLN3, CLN5, CLN6, CLN7, CLN8, CLN10, CLN12, PPT1, TPP1, MFSD8, and DNAJC5.
Test Cost and Sample Condition
The cost of the NCL Enzyme Panel NGS Genetic DNA Test is AED 4400.0. We accept blood samples or extracted DNA for this test. Alternatively, you can provide us with one drop of blood on an FTA card.
Report Delivery and Test Method
After the sample is collected, the report will be delivered to you within 3 to 4 weeks. Our NCL Enzyme Panel NGS Genetic DNA Test utilizes NGS technology, ensuring accurate and reliable results.
Test Type and Doctor’s Involvement
The NCL Enzyme Panel NGS Genetic DNA Test falls under the category of metabolic disorders. It is typically ordered by general physicians who suspect NCL or have patients with a family history of the disorder. Prior to the test, a genetic counseling session may be conducted to gather the clinical history of the patient and create a pedigree chart of affected family members.
Why Choose the NCL Enzyme Panel NGS Genetic DNA Test?
If you or your loved one is experiencing symptoms of NCL or has a family history of the disorder, the NCL Enzyme Panel NGS Genetic DNA Test can provide crucial information for diagnosis and treatment. Identifying mutations in the associated genes can help guide healthcare providers in developing a personalized management plan.
Don’t wait any longer. Contact DNA Labs UAE today to schedule your NCL Enzyme Panel NGS Genetic DNA Test and take control of your health.
| Test Name | NCL Enzyme Panel NGS Genetic DNA 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 NCL Enzyme Panel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NCL Enzyme Panel |
| Test Details | The NCL Enzyme Panel NGS Genetic DNA Test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze a group of genes associated with lysosomal storage disorders (LSDs) known as neuronal ceroid lipofuscinoses (NCLs). LSDs are a group of inherited disorders that result from the body’s inability to break down certain substances within cells. NCLs specifically affect the nervous system and can lead to progressive neurological decline, seizures, and vision loss. The NCL Enzyme Panel NGS Genetic DNA Test analyzes the DNA of an individual to identify mutations or changes in the genes associated with NCLs. This test can identify mutations in up to 13 genes that are known to cause NCLs, including CLN1, CLN2, CLN3, CLN5, CLN6, CLN7, CLN8, CLN10, CLN12, PPT1, TPP1, MFSD8, and DNAJC5. This test is typically ordered by a healthcare provider for individuals who have symptoms of an NCL or who have a family history of the disorder. Results from the test can help diagnose an NCL and guide treatment and management of the disorder. |
