FANCC Gene Fanconi Anemia Type C Genetic Test
At DNA Labs UAE, we offer the FANCC Gene Fanconi Anemia Type C Genetic Test. This test is designed to detect the presence of the FANCC gene mutation, which is associated with Fanconi anemia type C. Fanconi anemia type C is a rare genetic disorder that affects the bone marrow and increases the risk of certain cancers.
Test Components and Price
The FANCC Gene Fanconi Anemia Type C Genetic Test is priced at 4400.0 AED. The test requires a sample of blood or extracted DNA, or one drop of blood on an FTA Card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next Generation Sequencing) technology, which allows for the analysis of multiple genes simultaneously.
Test Type and Doctor
The FANCC Gene Fanconi Anemia Type C Genetic Test falls under the category of Metabolic Disorders. It is recommended to consult with a General Physician for this test.
Test Department and Pre Test Information
The test is conducted by our Genetics department. Before undergoing the FANCC Gene Fanconi Anemia Type C NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by Fanconi anemia type C.
Test Details
The FANCC gene is directly associated with Fanconi anemia type C. This rare genetic disorder affects the bone marrow and increases the risk of certain cancers. The FANCC Gene NGS Genetic Test involves obtaining a DNA sample, typically through blood or saliva, and sequencing the DNA to identify any variations or mutations in the FANCC gene. This test aids in the diagnosis of Fanconi anemia type C and determines the specific genetic mutation causing the disorder.
NGS genetic testing is a highly accurate and efficient method that allows for the analysis of multiple genes simultaneously. It can detect both small and large genetic variations, including single nucleotide changes, insertions, deletions, and gene rearrangements. Identifying a mutation in the FANCC gene through NGS genetic testing provides valuable information for diagnosis, genetic counseling, and treatment options.
Additionally, this test can help identify carriers of the gene mutation within a family and assist in family planning decisions. It is crucial to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.
At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. If you suspect Fanconi anemia type C or have a family history of the disorder, we encourage you to consult with a healthcare professional and consider the FANCC Gene Fanconi Anemia Type C Genetic Test.
| Test Name | FANCC Gene Fanconi anemia type C 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 FANCC Gene Fanconi anemia type C NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type C |
| Test Details |
The FANCC gene is associated with Fanconi anemia type C, which is a rare genetic disorder that affects the bone marrow and increases the risk of certain cancers. NGS (Next Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. A FANCC gene NGS genetic test 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 FANCC gene. This test can help diagnose Fanconi anemia type C and determine the specific genetic mutation causing the disorder. NGS genetic testing is a highly accurate and efficient method that allows for the analysis of multiple genes simultaneously. It can detect both small and large genetic variations, including single nucleotide changes, insertions, deletions, and gene rearrangements. If a mutation in the FANCC gene is identified through NGS genetic testing, it can provide valuable information for diagnosis, genetic counseling, and treatment options. It can also help identify carriers of the gene mutation within a family and assist in family planning decisions. It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate counseling and support. |
