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By what is called as amniocentesis, you can diagnose the chromosomal abnormality of the unborn baby. You do this procedure under cover of ultrasonography. The fetal cells will give you complete picture of the chromosomal abnormality of the unborn child.

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11y ago

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What factors most affect Chromosomal abnormalities?

Factors that most affect chromosomal abnormalities include advanced parental age, exposure to certain environmental toxins or radiation, and genetic predisposition. Additionally, errors during cell division or replication can also lead to chromosomal abnormalities.


What is meant by non-chromosomal congenital defects?

Non-chromosomal congenital defects refer to conditions or abnormalities that are not caused by changes in the person's chromosomes. These defects can result from a variety of factors such as exposure to toxins, infections during pregnancy, or unknown genetic mutations.


Are chromosomal abnormalities confined to certain parts of the body?

Chromosomal abnormalities can affect any cell in the body since they involve changes in the genetic material that is present in every cell. However, the impact of these abnormalities can vary depending on which chromosomes are affected and the specific genes involved.


What environmental factors may increase the incidence of chromosomal abnormalities?

Environmental factors that may increase the incidence of chromosomal abnormalities include exposure to radiation, pollutants, and certain chemicals, such as heavy metals and pesticides. Maternal factors like advanced age and exposure to teratogens during pregnancy can also contribute. Additionally, lifestyle choices such as smoking and excessive alcohol consumption are linked to higher rates of chromosomal abnormalities. These factors can disrupt normal cellular processes and lead to errors in DNA replication and repair.


What is anomaly scan?

abnormalities in ovaries during pregnancy


What is the cause of chromosomal?

Chromosomal disorders are caused by abnormalities in the chromosomes.


What causes body abnormalities?

Body abnormalities can arise from a variety of factors, including genetic mutations, environmental influences, and developmental issues during pregnancy. Genetic disorders, such as chromosomal abnormalities or single-gene mutations, can lead to physical differences. Additionally, exposure to harmful substances (teratogens) during critical stages of development, as well as nutritional deficiencies, can contribute to these abnormalities. Lastly, certain medical conditions and infections can also impact normal bodily development.


What is the causes of chromosomal disorder?

Chromosomal disorders can be caused by errors in cell division during meiosis or mitosis, exposure to certain environmental factors, such as radiation or chemicals, or by inheriting abnormal chromosomes from parents. These disorders can result in missing, extra, or scrambled genetic information, leading to a variety of physical and developmental abnormalities.


Which technique is used to collect fetal cells during pregnancy for genetic testing?

Chorionic villus sampling (CVS) involves collecting cells from the placenta, while amniocentesis involves collecting cells from the amniotic fluid surrounding the fetus. These tests can be done during pregnancy to obtain fetal cells for genetic testing and detecting chromosomal abnormalities.


Which test is carried out 15 to 20 weeks into the pregnancy and allows the analysis of fetal cells that can identify a variety of genetic defects with nearly 100 percent?

Amniocentesis is the test carried out during 15 to 20 weeks into pregnancy to analyze fetal cells for genetic defects. It provides a nearly 100% accuracy in identifying a variety of genetic conditions and chromosomal abnormalities.


What statement best describes the technique know as amniocentesis?

Amniocentesis is a procedure in which a small amount of amniotic fluid is extracted from the amniotic sac surrounding the fetus for testing. It is commonly used during pregnancy to detect genetic abnormalities, chromosomal disorders, and other potential health issues in the fetus. The procedure is typically done between 14 and 20 weeks of pregnancy.


Identify 3 causes of chromosomal disorders?

Chromosomal rearrangements, such as deletions, duplications, inversions, and translocations, can lead to chromosomal disorders. Errors in meiosis during gamete formation can result in abnormal chromosome numbers, such as trisomy (three copies) or monosomy (one copy). Exposure to environmental factors, such as radiation or certain chemicals, can increase the risk of chromosomal abnormalities.