Cystic Fibrosis CFTR Full Gene Sequence Analysis Test
Welcome to DNA Labs UAE, where we offer the Cystic Fibrosis CFTR full gene sequence analysis Test. This comprehensive genetic test can provide valuable information for individuals and families affected by Cystic Fibrosis (CF).
Test Details
Cystic Fibrosis (CF) is a genetic disorder that affects the lungs, pancreas, and other organs. CF is caused by mutations in the CFTR gene, which encodes a protein that regulates the transport of salt and water in and out of cells. CFTR full gene sequence analysis is a genetic test that examines the entire CFTR gene to identify mutations that can cause CF.
The test can detect all known CFTR mutations, including rare and novel variants. CFTR full gene sequence analysis is the most comprehensive genetic test for CF and is recommended for individuals with a family history of CF or symptoms suggestive of CF.
Test Components
- Sterile container
- Sterile Normal Saline Container
- EDTA Vacutainer
Test Price
The cost of the Cystic Fibrosis CFTR full gene sequence analysis Test is 4400.0 AED.
Sample Condition
The test can be performed using Amniotic fluid, Chorionic villi, or Peripheral blood samples.
Report Delivery
The test results will be delivered within 4-6 weeks.
Method
The Cystic Fibrosis CFTR full gene sequence analysis Test is performed using Next-Generation Sequencing (NGS) technology.
Test Type
The test falls under the category of Genetics.
Doctor
The test can be ordered by a General Physician.
Test Department
The test is conducted in our dedicated Test Department.
Pre Test Information
Cystic Fibrosis: CFTR full gene sequence analysis can be done with a doctor’s prescription. However, please note that the prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Summary
In summary, the Cystic Fibrosis CFTR full gene sequence analysis Test is a comprehensive genetic test that can identify mutations in the CFTR gene that cause CF. The test is recommended for individuals with a family history of CF or symptoms suggestive of CF. It can provide valuable information for diagnosis, family planning, and clinical management of CF.
| Test Name | Cystic Fibrosis CFTR full gene sequence analysis Test |
|---|---|
| Components | Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer |
| Price | 4400.0 AED |
| Sample Condition | Amniotic fluid\/ Chorionic villi\/ Peripheral blood |
| Report Delivery | 4-6 weeks |
| Method | NGS |
| Test type | Genetics |
| Doctor | General Physician |
| Test Department: | |
| Pre Test Information | Cystic Fibrosis: CFTR full gene sequence analysis can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
| Test Details | Cystic Fibrosis (CF) is a genetic disorder that affects the lungs, pancreas, and other organs. CF is caused by mutations in the CFTR gene, which encodes a protein that regulates the transport of salt and water in and out of cells. CFTR mutations can result in the production of a defective protein, which leads to the accumulation of thick, sticky mucus in the lungs and other organs. CFTR full gene sequence analysis is a genetic test that examines the entire CFTR gene to identify mutations that can cause CF. The test can detect all known CFTR mutations, including rare and novel variants. CFTR full gene sequence analysis is the most comprehensive genetic test for CF and is recommended for individuals with a family history of CF or symptoms suggestive of CF. CFTR full gene sequence analysis is performed using a blood or saliva sample. The DNA is extracted from the sample and then amplified using polymerase chain reaction (PCR). The amplified DNA is then sequenced using next-generation sequencing (NGS) technology. The resulting sequence data is analyzed to identify any mutations in the CFTR gene. CFTR full gene sequence analysis can provide valuable information for individuals and families affected by CF. The test can confirm a diagnosis of CF, identify carriers of CF mutations, and provide information for family planning. It can also help guide treatment decisions and inform clinical management of CF. In summary, CFTR full gene sequence analysis is a comprehensive genetic test that can identify mutations in the CFTR gene that cause CF. The test is recommended for individuals with a family history of CF or symptoms suggestive of CF. It can provide valuable information for diagnosis, family planning, and clinical management of CF. |
