FANCF Gene Fanconi Anemia Type F Genetic Test
At DNA Labs UAE, we offer the FANCF Gene Fanconi anemia type F Genetic Test at a cost of AED 4400.0. This test is designed to diagnose Fanconi anemia type F, a rare genetic disorder characterized by bone marrow failure, physical abnormalities, and an increased risk of cancer.
Test Details
The FANCF gene is associated with Fanconi anemia type F. Our NGS (Next-Generation Sequencing) technology allows for the simultaneous analysis of multiple genes, making it an effective method for identifying mutations or variations in the FANCF gene that may be responsible for the disorder.
To perform the test, we require a DNA sample, which can be obtained through a blood or saliva sample. The DNA is then sequenced to identify any variations or mutations in the FANCF gene. This information can help in the diagnosis of Fanconi anemia type F and guide treatment decisions and genetic counseling for affected individuals and their families.
It’s important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.
Test Components and Price
The FANCF Gene Fanconi anemia type F Genetic Test costs AED 4400.0. The test requires a blood or extracted DNA sample, or one drop of blood on an FTA Card.
Report Delivery
The test results will be delivered within 3 to 4 weeks.
Test Type and Department
The FANCF Gene Fanconi anemia type F Genetic Test falls under the category of Metabolic Disorders. It is conducted in our Genetics department.
Referring Doctor
The test can be requested by a General Physician.
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient who is going for the FANCF Gene Fanconi anemia type F NGS Genetic DNA Test. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected with Fanconi anemia type F.
| Test Name | FANCF Gene Fanconi anemia type F 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 FANCF Gene Fanconi anemia type F NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type F |
| Test Details |
The FANCF gene is associated with Fanconi anemia type F, which is a rare genetic disorder characterized by bone marrow failure, physical abnormalities, and an increased risk of cancer. NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes. In the context of Fanconi anemia type F, NGS genetic testing can be used to identify mutations or variations in the FANCF gene that may be responsible for the disorder. NGS genetic testing typically involves obtaining a DNA sample, usually through a blood or saliva sample, and then sequencing the DNA to identify any variations or mutations in the FANCF gene. This information can help in the diagnosis of Fanconi anemia type F and may also guide treatment decisions and genetic counseling for affected individuals and their families. It’s important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support. |
