CHROMOSOME ANALYSIS CHORIONIC VILLUS Test
Test Name: CHROMOSOME ANALYSIS CHORIONIC VILLUS Test
Test Components: Chromosome analysis of chorionic villus cells
Price: 2570.0 AED
Sample Condition: 40 mg (20 mg min.) Chorionic villus biopsy collected aseptically in 10 mL transport medium available from LPL. Sample to be collected under strict aseptic precautions. Ship refrigerated immediately. DO NOT FREEZE.
Specimen Delivery: Sample must reach LPL New Delhi within 48 hours.
Recommended Gestation Period: 10-13 weeks
Required Forms: Duly filled Chromosome & FISH Analysis Requisition form (Form 17) & Consent form (Form 18) for Prenatal Genetic Testing
Report Delivery: Sample Daily by 6 pm; Report 21 Working days
Method: Culture, Microscopy, Karyotype
Test Type: Prenatal Diagnosis
Referring Doctor: Gynecologist
Test Department: CYTOGENETICS
Pre Test Information: Test is recommended between 10-13 weeks of gestation. Duly filled Chromosome & FISH Analysis Requisition form (Form 17) & Consent form (Form 18) for Prenatal Genetic Testing is mandatory.
Test Details
Chromosome analysis of chorionic villus (CV) cells is a prenatal diagnostic test that is performed to detect genetic abnormalities in a developing fetus. It involves the sampling of cells from the chorionic villi, which are tiny finger-like projections on the placenta that provide nutrients to the fetus.
The test is typically performed between 10-13 weeks of pregnancy and can be done through two methods: transcervical or transabdominal. In the transcervical method, a thin tube is inserted through the cervix to collect a small sample of the chorionic villi. In the transabdominal method, a needle is inserted through the abdomen to reach the placenta and collect the sample.
Once the sample is obtained, the cells are analyzed in a laboratory. The chromosomes are examined to check for any numerical or structural abnormalities. This can help identify conditions such as Down syndrome, Edwards syndrome, Patau syndrome, and other chromosomal disorders.
Chromosome analysis of chorionic villus cells is considered a highly accurate test for detecting genetic abnormalities. However, it is an invasive procedure and carries a small risk of complications, including miscarriage. Therefore, it is usually recommended for women who have an increased risk of having a baby with a genetic disorder or those who have received abnormal results from other prenatal screening tests.
It is important to discuss the risks, benefits, and limitations of the test with a healthcare provider before deciding to undergo chromosome analysis of chorionic villus cells.
| Test Name | CHROMOSOME ANALYSIS CHORIONIC VILLUS Test |
|---|---|
| Components | |
| Price | 2570.0 AED |
| Sample Condition | 40 mg (20 mg min.) Chorionic villus biopsy collected aseptically in 10 mL transport medium available from LPL. Sample to be collected under strict aseptic precautions. Ship refrigerated immediately. DO NOT FREEZE.Specimen must reach LPL New Delhi within 48 hours.Test is recommended between 10-13 weeks of gestation. Duly filledChromosome & FISH Analysis Requisition form (Form 17) & Consent form (Form 18) for Prenatal Genetic Testing is mandatory. |
| Report Delivery | Sample Daily by 6 pm; Report 21 Working days |
| Method | Culture, Microscopy, Karyotype |
| Test type | Prenatal Diagnosis |
| Doctor | Gynecologist |
| Test Department: | CYTOGENETICS |
| Pre Test Information | Test is recommended between 10-13 weeks of gestation. Duly filledChromosome & FISH Analysis Requisition form (Form 17) & Consent form (Form 18) for Prenatal Genetic Testing is mandatory. |
| Test Details |
Chromosome analysis of chorionic villus (CV) cells is a prenatal diagnostic test that is performed to detect genetic abnormalities in a developing fetus. It involves the sampling of cells from the chorionic villi, which are tiny finger-like projections on the placenta that provide nutrients to the fetus. The test is typically performed between 10-13 weeks of pregnancy and can be done through two methods: transcervical or transabdominal. In the transcervical method, a thin tube is inserted through the cervix to collect a small sample of the chorionic villi. In the transabdominal method, a needle is inserted through the abdomen to reach the placenta and collect the sample. Once the sample is obtained, the cells are analyzed in a laboratory. The chromosomes are examined to check for any numerical or structural abnormalities. This can help identify conditions such as Down syndrome, Edwards syndrome, Patau syndrome, and other chromosomal disorders. Chromosome analysis of chorionic villus cells is considered a highly accurate test for detecting genetic abnormalities. However, it is an invasive procedure and carries a small risk of complications, including miscarriage. Therefore, it is usually recommended for women who have an increased risk of having a baby with a genetic disorder or those who have received abnormal results from other prenatal screening tests. It is important to discuss the risks, benefits, and limitations of the test with a healthcare provider before deciding to undergo chromosome analysis of chorionic villus cells. |
