PCCB Gene Propionic acidemia Genetic Test
At DNA Labs UAE, we offer the PCCB Gene Propionic acidemia Genetic Test at a cost of 4400.0 AED.
Test Details
The PCCB (propionyl-CoA carboxylase beta subunit) gene is associated with a genetic disorder called propionic acidemia. Propionic acidemia is an inherited metabolic disorder characterized by the inability to break down certain proteins and fats properly. This leads to the buildup of toxic substances, including propionic acid, in the body.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of propionic acidemia, NGS genetic testing can be used to identify mutations or variations in the PCCB gene that may be responsible for the disorder.
By analyzing the PCCB gene using NGS technology, healthcare professionals can determine if there are any mutations or variations present that could be causing propionic acidemia. This information can be helpful in diagnosing the disorder, predicting the severity of symptoms, and providing appropriate treatment and management strategies.
It is important to note that NGS genetic testing for propionic acidemia is typically performed in a specialized laboratory and requires a healthcare professional’s order. The results of the test should be interpreted by a genetic counselor or medical geneticist who can provide guidance and support to individuals and families affected by the disorder.
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
Prior to undergoing the PCCB Gene Propionic acidemia Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with Propionic acidemia.
| Test Name | PCCB Gene Propionic acidemia 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for PCCB Gene Propionic acidemia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Propionic acidemia |
| Test Details |
PCCB (propionyl-CoA carboxylase beta subunit) gene is associated with a genetic disorder called propionic acidemia. Propionic acidemia is an inherited metabolic disorder characterized by the inability to break down certain proteins and fats properly. This leads to the buildup of toxic substances, including propionic acid, in the body. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of propionic acidemia, NGS genetic testing can be used to identify mutations or variations in the PCCB gene that may be responsible for the disorder. By analyzing the PCCB gene using NGS technology, healthcare professionals can determine if there are any mutations or variations present that could be causing propionic acidemia. This information can be helpful in diagnosing the disorder, predicting the severity of symptoms, and providing appropriate treatment and management strategies. It is important to note that NGS genetic testing for propionic acidemia is typically performed in a specialized laboratory and requires a healthcare professional’s order. The results of the test should be interpreted by a genetic counselor or medical geneticist who can provide guidance and support to individuals and families affected by the disorder. |
