FISH FOR PRE or POSTNATAL DIAGNOSIS CHROMOSOME 13 21 Test
At DNA Labs UAE, we offer the FISH for Pre or Postnatal Diagnosis Chromosome 13 21 Test for AED 1530.0. This test is specifically designed for aneuploidy detection of Trisomy 13 and 21.
Test Details
The FISH analysis, also known as fluorescence in situ hybridization, is a molecular cytogenetic technique used for the detection of chromosomal abnormalities. It involves the use of fluorescently labeled DNA probes that specifically bind to target DNA sequences on chromosomes.
For prenatal diagnosis, FISH analysis can be used to detect chromosomal abnormalities in the developing fetus. It is often performed on cells obtained through chorionic villus sampling (CVS) or amniocentesis. In the case of chromosome 13 or 21 abnormalities, FISH analysis can be used to specifically identify trisomy 13 (also known as Patau syndrome) or trisomy 21 (also known as Down syndrome).
In postnatal diagnosis, FISH analysis can be used to confirm the presence of chromosomal abnormalities in individuals who exhibit clinical features suggestive of a particular syndrome. It can be performed on various types of samples, including blood, skin, or tissue samples.
Overall, FISH analysis is a valuable tool for the pre or postnatal diagnosis of chromosomal abnormalities, including those involving chromosome 13 or 21. It provides rapid and accurate results, allowing for timely medical intervention and genetic counseling.
Test Information
- Test Name: FISH FOR PRE or POSTNATAL DIAGNOSIS CHROMOSOME 13 21 Test
- Components: Aneuploidy detection for Trisomy 13 21
- Price: 1530.0 AED
- Sample Condition:
- Report Delivery: 10-12 days
- Method: FISH
- Test Type: Gynecology
- Doctor: Gynecologist
- Test Department: Cytogenetics
Pre Test Information
To be used as a prenatal screen, in conjunction with chromosome analysis, to detect aneuploidy such as Trisomies 13 21.
| Test Name | FISH FOR PRE or POSTNATAL DIAGNOSIS CHROMOSOME 13 21 Test |
|---|---|
| Components | Aneuploidy detection for Trisomy 13 21 |
| Price | 1530.0 AED |
| Sample Condition | |
| Report Delivery | 10-12 days |
| Method | FISH |
| Test type | Gynecology |
| Doctor | Gynecologist |
| Test Department: | Cytogenetics |
| Pre Test Information | To be used as a prenatal screen, in conjunction with chromosome analysis, to detect aneuploidy such as Trisomies 13 21 |
| Test Details | Fish analysis, also known as fluorescence in situ hybridization, is a molecular cytogenetic technique used for the detection of chromosomal abnormalities. It involves the use of fluorescently labeled DNA probes that specifically bind to target DNA sequences on chromosomes. For prenatal diagnosis, FISH analysis can be used to detect chromosomal abnormalities in the developing fetus. It is often performed on cells obtained through chorionic villus sampling (CVS) or amniocentesis. In the case of chromosome 13 or 21 abnormalities, FISH analysis can be used to specifically identify trisomy 13 (also known as Patau syndrome) or trisomy 21 (also known as Down syndrome). In postnatal diagnosis, FISH analysis can be used to confirm the presence of chromosomal abnormalities in individuals who exhibit clinical features suggestive of a particular syndrome. It can be performed on various types of samples, including blood, skin, or tissue samples. Overall, FISH analysis is a valuable tool for the pre or postnatal diagnosis of chromosomal abnormalities, including those involving chromosome 13 or 21. It provides rapid and accurate results, allowing for timely medical intervention and genetic counseling. |
