FANCE Gene Fanconi Anemia Type E Genetic Test
Test Name: FANCE Gene Fanconi anemia type E Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 FANCE Gene Fanconi anemia type E NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type E.
About FANCE Gene Fanconi Anemia Type E Genetic Test
The FANCE gene is associated with Fanconi anemia type E, a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer.
NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous sequencing of multiple genes, including the FANCE gene. It can identify specific mutations or variants within the FANCE gene that may be responsible for causing Fanconi anemia type E.
By performing an NGS genetic test for the FANCE gene, healthcare professionals can accurately diagnose individuals with Fanconi anemia type E and provide appropriate medical management and genetic counseling.
Additionally, this test can be useful for carrier screening in families with a history of Fanconi anemia type E, allowing for informed family planning decisions.
Test Name | FANCE Gene Fanconi anemia type E 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 FANCE Gene Fanconi anemia type E NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type E |
Test Details |
The FANCE gene is associated with Fanconi anemia type E, which is a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer. NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous sequencing of multiple genes, including the FANCE gene. It can identify specific mutations or variants within the FANCE gene that may be responsible for causing Fanconi anemia type E. By performing an NGS genetic test for the FANCE gene, healthcare professionals can accurately diagnose individuals with Fanconi anemia type E and provide appropriate medical management and genetic counseling. Additionally, this test can be useful for carrier screening in families with a history of Fanconi anemia type E, allowing for informed family planning decisions. |