PDGFB Gene Basal Ganglia Calcification Type 5 Idiopathic Genetic Test
Welcome to DNA Labs UAE, where we offer the PDGFB Gene Basal Ganglia Calcification Type 5 Idiopathic Genetic Test. This test is designed to detect mutations or variations in the PDGFB gene associated with basal ganglia calcification type 5, also known as Fahr’s disease.
Test Components
The PDGFB Gene Basal Ganglia Calcification Type 5 Idiopathic Genetic Test includes the following 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: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Prior to undergoing the PDGFB Gene Basal Ganglia Calcification Type 5 Idiopathic 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 PDGFB Gene Basal Ganglia Calcification Type 5. This will help in understanding the inheritance pattern and identifying potential carriers of the gene.
Test Details
The PDGFB gene basal ganglia calcification type 5 idiopathic NGS genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the PDGFB gene for any mutations or variations. Basal ganglia calcification is a condition characterized by the abnormal deposition of calcium in the brain, specifically in the basal ganglia region.
Identifying mutations or variations in the PDGFB gene can aid in confirming a diagnosis of basal ganglia calcification type 5 and provide information about the risk of developing the condition or passing it on to future generations. This genetic test is an important tool in understanding the genetic basis of basal ganglia calcification and can assist in making informed medical decisions.
For more information about the PDGFB Gene Basal Ganglia Calcification Type 5 Idiopathic Genetic Test or to schedule an appointment, please contact DNA Labs UAE.
Test Name | PDGFB Gene Basal ganglia calcification type 5 idiopathic 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 | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for PDGFB Gene Basal ganglia calcification type 5, idiopathic NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDGFB Gene Basal ganglia calcification type 5, idiopathic NGS Genetic DNA Test gene PDGFB |
Test Details |
PDGFB gene basal ganglia calcification type 5, idiopathic NGS genetic test is a type of genetic test that is used to detect mutations or variations in the PDGFB gene that are associated with basal ganglia calcification type 5 (also known as Fahr’s disease). Basal ganglia calcification is a condition characterized by the abnormal deposition of calcium in the brain, specifically in the basal ganglia region. This genetic test uses Next-Generation Sequencing (NGS) technology to analyze the PDGFB gene and identify any mutations or variations that may be present. Identifying these genetic changes can help in confirming a diagnosis of basal ganglia calcification type 5 and may also provide information about the risk of developing the condition or the likelihood of passing it on to future generations. |