William’s Syndrome FISH Test
Test Name: William’s Syndrome FISH Test
Components: Sterile container / Sterile Normal Saline Container / Sodium heparin Vacutainer (2ml)
Price: 1050.0 AED
Sample Condition: Peripheral blood/Amniotic fluid/Chorionic villi/Cord blood
Report Delivery: 3-4 days
Method: FISH
Test Type: Genetics
Doctor: Oncology
Test Department: DNA Labs UAE
Pre Test Information: William’s Syndrome (FISH) can be done with a doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Test Details
FISH stands for Fluorescence In Situ Hybridization, which is a laboratory technique used to detect and locate specific DNA sequences on chromosomes. In the case of William’s Syndrome, FISH can be used to diagnose the condition by detecting a specific deletion on chromosome 7.
William’s Syndrome is a genetic disorder characterized by a variety of physical and intellectual features. It is caused by a deletion of genetic material on chromosome 7, specifically at the region known as 7q11.23. This deletion affects the production of certain proteins and leads to the characteristic features of the syndrome.
FISH testing involves the use of fluorescently labeled DNA probes that bind to specific DNA sequences on the chromosomes. In the case of William’s Syndrome, the FISH test uses a probe that binds to the region on chromosome 7 that is typically deleted in individuals with the syndrome. If the probe binds to the chromosome, it indicates the presence of the deletion and confirms the diagnosis of William’s Syndrome.
FISH testing is a highly accurate and specific method for diagnosing William’s Syndrome. It is usually performed on a blood sample and can provide results within a few days. In addition to diagnosing the condition, FISH testing can also be used to determine if a person is a carrier of the deletion, which can be important for family planning purposes.
| Test Name | William’s Syndrome FISH Test |
|---|---|
| Components | Sterile container / Sterile Normal Saline Container / Sodium heparin Vacutainer (2ml) |
| Price | 1050.0 AED |
| Sample Condition | Peripheral blood\/Amniotic fluid \/ Chorionic villi \/ Cord blood |
| Report Delivery | 3-4 days |
| Method | FISH |
| Test type | Genetics |
| Doctor | Oncology |
| Test Department: | |
| Pre Test Information | William’s Syndrome (FISH) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
| Test Details |
FISH stands for Fluorescence In Situ Hybridization, which is a laboratory technique used to detect and locate specific DNA sequences on chromosomes. In the case of William’s Syndrome, FISH can be used to diagnose the condition by detecting a specific deletion on chromosome 7. William’s Syndrome is a genetic disorder characterized by a variety of physical and intellectual features. It is caused by a deletion of genetic material on chromosome 7, specifically at the region known as 7q11.23. This deletion affects the production of certain proteins and leads to the characteristic features of the syndrome. FISH testing involves the use of fluorescently labeled DNA probes that bind to specific DNA sequences on the chromosomes. In the case of William’s Syndrome, the FISH test uses a probe that binds to the region on chromosome 7 that is typically deleted in individuals with the syndrome. If the probe binds to the chromosome, it indicates the presence of the deletion and confirms the diagnosis of William’s Syndrome. FISH testing is a highly accurate and specific method for diagnosing William’s Syndrome. It is usually performed on a blood sample and can provide results within a few days. In addition to diagnosing the condition, FISH testing can also be used to determine if a person is a carrier of the deletion, which can be important for family planning purposes. |
