Chromosome testing requires a blood test, which can help patients find out whether they suffer from infertility and habitual miscarriage. It can also help screen for certain genetic diseases and whether the fetus has malformations. 1 What is the chromosome test? Chromosome examination is done by drawing blood, specifically 0.5 ml of venous blood is inoculated into a specific culture medium, cells are harvested 68-72 hours later, stained for banding, magnified 1000 times under a microscope, and counted and analyzed for karyotype. 2 The significance of chromosomes The chromosomes of sperm and egg carry the genetic genes of the father and mother respectively, which record the genetic information passed from parents to their children. Similarly, when sex chromosomes are abnormal, genetic diseases can occur. Chromosomal abnormalities can cause oligospermia and azoospermia, accounting for 2% to 21% of male infertility. 3 The significance of chromosome examination Chromosome examination is mainly an important auxiliary examination method. It can not only check whether a woman suffers from infertility or habitual miscarriage, but also conduct prenatal screening, certain genetic diseases, and related examinations for hermaphroditism. It can quickly report chromosome test results, detect diseases as early as possible and provide treatment as early as possible to avoid serious consequences. 4 Who should undergo chromosome testing? Its main target groups are: couples with adverse pregnancy and delivery histories such as unexplained spontaneous abortion, stillbirth, neonatal death or teratozoa; couples with primary infertility; people with congenital malformations; people with mental retardation; people with abnormal growth and development; people with primary amenorrhea; people with incomplete sexual development or sexual malformations; patients with azoospermia, oligospermia, asthenospermia or teratospermia. Its main technical means are various chromosome banding analyses. |
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