PDGFRB Gene Basal Ganglia Calcification Type 4 Genetic Test sale cost 4400 AED
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PDGFRB Gene Basal Ganglia Calcification Type 4 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The “PDGFRB Gene Basal Ganglia Calcification Type 4 Genetic Test” is a specialized diagnostic tool designed to detect mutations in the PDGFRB gene, which are implicated in Basal Ganglia Calcification Type 4, also known as Primary Familial Brain Calcification (PFBC) Type 4. This condition is characterized by the accumulation of calcium deposits in the basal ganglia, a critical part of the brain involved in regulating movement, which can lead to a range of neurological symptoms including movement disorders, psychiatric symptoms, and cognitive impairment.

The test is particularly valuable for individuals who have a family history of PFBC or who exhibit symptoms suggestive of basal ganglia calcification. Early detection through genetic testing can aid in the diagnosis, management, and understanding of the condition, potentially guiding treatment options and genetic counseling.

Performed at DNA Labs UAE, a reputable genetic testing facility, the test cost is set at 4400 AED. DNA Labs UAE employs state-of-the-art genetic sequencing technologies to ensure accurate and reliable results, providing crucial information for affected individuals and their families. This genetic test represents a critical step towards personalized medicine in the management of PFBC Type 4, offering hope and clarity for those affected by this rare condition.

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PDGFRB Gene Basal Ganglia Calcification Type 4 Genetic Test

Components: PDGFRB Gene Basal ganglia calcification 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: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for PDGFRB Gene Basal ganglia calcification type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDGFRB Gene Basal ganglia calcification type 4 NGS Genetic DNA Test gene PDGFRB

Test Details: PDGFRB gene basal ganglia calcification type 4 NGS genetic test is a type of genetic test that is used to detect mutations or variations in the PDGFRB gene that are associated with basal ganglia calcification type 4. Basal ganglia calcification, also known as Fahr’s disease, is a rare genetic disorder characterized by the abnormal accumulation of calcium in the basal ganglia and other brain regions. The PDGFRB gene provides instructions for making a protein called platelet-derived growth factor receptor beta. This protein plays a role in cell growth, division, and survival. Mutations in the PDGFRB gene can disrupt the normal function of the protein, leading to the development of basal ganglia calcification type 4. NGS, or next-generation sequencing, is a high-throughput DNA sequencing technology that allows for the rapid and simultaneous sequencing of multiple genes or even entire genomes. In the context of genetic testing, NGS can be used to analyze the entire coding region of the PDGFRB gene to identify any mutations or variations that may be present. By performing a PDGFRB gene basal ganglia calcification type 4 NGS genetic test, healthcare professionals can determine if an individual has any mutations or variations in the PDGFRB gene that are associated with basal ganglia calcification type 4. This information can be used for diagnosis, genetic counseling, and potentially for developing personalized treatment approaches in the future.

Test Name PDGFRB Gene Basal ganglia calcification type 4 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 PDGFRB Gene Basal ganglia calcification type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDGFRB Gene Basal ganglia calcification type 4 NGS Genetic DNA Test gene PDGFRB
Test Details

PDGFRB gene basal ganglia calcification type 4 NGS genetic test is a type of genetic test that is used to detect mutations or variations in the PDGFRB gene that are associated with basal ganglia calcification type 4. Basal ganglia calcification, also known as Fahr’s disease, is a rare genetic disorder characterized by the abnormal accumulation of calcium in the basal ganglia and other brain regions.

The PDGFRB gene provides instructions for making a protein called platelet-derived growth factor receptor beta. This protein plays a role in cell growth, division, and survival. Mutations in the PDGFRB gene can disrupt the normal function of the protein, leading to the development of basal ganglia calcification type 4.

NGS, or next-generation sequencing, is a high-throughput DNA sequencing technology that allows for the rapid and simultaneous sequencing of multiple genes or even entire genomes. In the context of genetic testing, NGS can be used to analyze the entire coding region of the PDGFRB gene to identify any mutations or variations that may be present.

By performing a PDGFRB gene basal ganglia calcification type 4 NGS genetic test, healthcare professionals can determine if an individual has any mutations or variations in the PDGFRB gene that are associated with basal ganglia calcification type 4. This information can be used for diagnosis, genetic counseling, and potentially for developing personalized treatment approaches in the future.

SKU: TEST-4002 Category:

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