C19orf12 Gene Neurodegeneration with brain iron accumulation type 4 Genetic Test
Welcome to DNA Labs UAE’s blog on the C19orf12 Gene Neurodegeneration with brain iron accumulation type 4 Genetic Test. In this blog, we will discuss the symptoms, diagnosis, and cost of this test.
Test Details
The C19orf12 gene is associated with a neurodegenerative disorder known as neurodegeneration with brain iron accumulation type 4 (NBIA4). NBIA4 is a rare genetic disorder characterized by abnormal iron accumulation in the brain, which leads to progressive neurological symptoms.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. For NBIA4, NGS genetic testing can identify mutations or variants in the C19orf12 gene that may be responsible for the disorder.
The NGS genetic test for NBIA4 requires a sample of DNA, typically collected through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to analyze the C19orf12 gene and other relevant genes associated with NBIA4.
The results of the test can confirm a diagnosis of NBIA4 and provide information about the specific genetic variant(s) present. This test is particularly helpful for individuals with symptoms of the disorder and their family members who may be at risk of inheriting the condition.
Test Components and Price
- Test Name: C19orf12 Gene Neurodegeneration with brain iron accumulation type 4 Genetic Test
- 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
Prior to undergoing the C19orf12 Gene Neurodegeneration with brain iron accumulation type 4 NGS Genetic DNA 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 NBIA4.
Importance of Genetic Testing
Genetic testing for NBIA4 can provide valuable information for genetic counseling, family planning, and potential treatment options. It is essential to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor, who can provide appropriate counseling and support throughout the testing process.
By offering the C19orf12 Gene Neurodegeneration with brain iron accumulation type 4 Genetic Test, DNA Labs UAE aims to assist individuals and their families in understanding and managing this rare genetic disorder.
| Test Name | C19orf12 Gene Neurodegeneration with brain iron accumulation type 4 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 C19orf12 Gene Neurodegeneration with brain iron accumulation type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with C19orf12 Gene Neurodegeneration with brain iron accumulation type 4 |
| Test Details |
C19orf12 is a gene that is associated with a neurodegenerative disorder called neurodegeneration with brain iron accumulation type 4 (NBIA4). NBIA4 is a rare genetic disorder characterized by abnormal iron accumulation in the brain, leading to progressive neurological symptoms. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of NBIA4, NGS genetic testing can be used to identify mutations or variants in the C19orf12 gene that may be responsible for the disorder. The NGS genetic test for NBIA4 involves collecting a sample of DNA, usually through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to analyze the C19orf12 gene and other relevant genes associated with NBIA4. The results of the test can help confirm a diagnosis of NBIA4 and provide information about the specific genetic variant(s) present. Genetic testing for NBIA4 can be helpful for individuals with symptoms of the disorder, as well as their family members who may be at risk of inheriting the condition. It can provide valuable information for genetic counseling, family planning, and potential treatment options. It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor, who can provide appropriate counseling and support throughout the testing process. |
