BRIP1 Gene Fanconi anemia type J Genetic Test
Cost: AED 4400.0
Test Components:
- Price: AED 4400.0
- 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 BRIP1 Gene Fanconi anemia type J NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type J
Test Details:
The BRIP1 gene is associated with Fanconi anemia type J, a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify any mutations or variations in the DNA sequence.
NGS genetic testing for the BRIP1 gene in individuals suspected of having Fanconi anemia type J involves obtaining a DNA sample, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology, which allows for the analysis of the entire BRIP1 gene sequence. The test can identify any variations or mutations in the gene that may be causing the disease.
The results of the test can help confirm a diagnosis of Fanconi anemia type J in individuals with suspected symptoms or a family history of the disorder. It can also provide information about the specific mutation in the BRIP1 gene, which can be useful for genetic counseling and family planning.
It is important to note that NGS genetic testing may not detect all possible mutations or variations in the BRIP1 gene. Additionally, the interpretation of the test results requires expertise in genetics and should be done by a qualified healthcare professional or genetic counselor.
| Test Name | BRIP1 Gene Fanconi anemia type J 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 BRIP1 Gene Fanconi anemia type J NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type J |
| Test Details |
The BRIP1 gene is associated with Fanconi anemia type J, a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify any mutations or variations in the DNA sequence. NGS genetic testing for the BRIP1 gene in individuals suspected of having Fanconi anemia type J involves obtaining a DNA sample, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology, which allows for the analysis of the entire BRIP1 gene sequence. The test can identify any variations or mutations in the gene that may be causing the disease. The results of the test can help confirm a diagnosis of Fanconi anemia type J in individuals with suspected symptoms or a family history of the disorder. It can also provide information about the specific mutation in the BRIP1 gene, which can be useful for genetic counseling and family planning. It is important to note that NGS genetic testing may not detect all possible mutations or variations in the BRIP1 gene. Additionally, the interpretation of the test results requires expertise in genetics and should be done by a qualified healthcare professional or genetic counselor. |
