Karyotyping test in India can be performed on a sample of blood, bone marrow, amniotic fluid, or tissue from the placenta, the organ that develops during pregnancy to feed a growing baby. To test amniotic fluid, an amniocentesis is done. A bone marrow specimen requires a bone marrow biopsy. The sample is placed into a special dish and allowed to grow in the laboratory. Cells are later taken from the growing sample and stained. The laboratory specialist uses a microscope to examine the size, shape, and number of chromosomes in the cell sample.
The stained sample is photographed to provide a karyotype, which shows the arrangement of the chromosomes. Certain abnormalities can be identified through the number or arrangement of the chromosomes. Chromosomes contain thousands of genes that are stored in DNA, the basic genetic material.
The stained cells are evaluated and assessed under a microscope for abnormalities; abnormalities can consist of –
The lab experts of We Care IVF Surrogacy examine the chromosome’ size, its shape and the number; this information is essential in evaluating any genetic abnormalities.
We Care India is one of the ongoing center that has gained the trust of n number of couples and has become the leading center providing the best diagnostic tests and any treatments associated with the couple’s fertility.
Abnormal number of chromosomes, the wrong way arranged chromosomes, or malformed chromosomes – these are some of the common signs of genetic situation. Genetic conditions varies greatly, examples are Turner syndrome and Down syndrome.
Karyotyping test in India is used to find out assortment of genetic disorders, take an instance of a woman, who has experienced premature ovarian failure- this failure could be of chromosomal defect and this defect can be detected by the way of Karyotyping test in India. This test is also considered best to identify the Philadelphia chromosome (the presence of this chromosome can pinpoint CML – Chronic Myelogenous Leukemia).
When you will receive the result of your Karyotyping test in India that means the report is of your baby’s chromosomes evaluation, so the outcomes are definite – either the baby is completely normal or the baby has genetic issue.
Abnormality or any issue detected by the karyotype test could be the result of any chromosomal disorder or genetic syndrome. The karyotype test in India sometimes is repeated to make sure regarding the presence of genetic issue.
Karyotyping Test in India is one of the prenatal screenings that scrutinizes certain genetic and chromosomal abnormalities. A woman will probably be recommended by the experts to do this test during her first trimester and also in the second trimester. The specialist will let the woman know which karyotype test will be suitable for her on the basis of how long she is the pregnancy days and on her risks. This test can only be carried out during certain weeks of the pregnancy.
Complications associated with this test are rare; a woman may experience slight possibility of bleeding, she may have infection from having the procedure of blood drawn or if the patient has undergone bone marrow biopsy. Amniocentesis carries a minor risk
With over 10 years experience and over 10,000+ successful live births through IVF, we are dedicated to hand out best fertility treatment and personalized nursing to accomplish couple’s parenthood soon.
26/18, West Patel Nagar, New Delhi
Kathmandu 44600, Nepal
19 A Dniprovska Kiev 02081, Ukraine
Tbilisi, Capital of Georgia