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chorionic villus sampling
(redirected from Chorionic Villi Sampling)

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chorionic villus sampling (CVS) or chorionic villus biopsy (CVB) (kōr'ē-ŏn`ĭk, kôr'–), diagnostic procedure in which a sample of chorionic villi from the developing placenta is removed from the uterus of a pregnant woman (see pregnancy pregnancy, period of time between fertilization of the ovum (conception) and birth, during which mammals carry their developing young in the uterus (see embryo). The duration of pregnancy in humans is about 280 days, equal to 9 calendar months.
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) using a fine needle inserted through the abdomen or a thin plastic catheter inserted into the vagina and through the cervix. Chorionic villi are fingerlike projections of a membrane (the chorion) that surrounds the fetus. The villi develop from the fertilized ovum ovum , in biology, specialized plant or animal sex cell, also called the egg, or egg cell. It is the female sex cell, or female gamete; the male gamete is the sperm. The study of the ovum is included in the science of embryology.
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, or egg, and have a genetic composition similar to that of the fetus. Cells in the sample are grown in the laboratory and studied to detect the presence in the fetus of such genetic birth defects birth defects, abnormalities in physical or mental structure or function that are present at birth. They range from minor to seriously deforming or life-threatening. A major defect of some type occurs in approximately 3% of all births.
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 as Tay-Sachs disease Tay-Sachs disease , rare hereditary disease caused by a genetic mutation that leaves the body unable to produce an enzyme necessary for fat metabolism in nerve cells, producing central nervous system degeneration.
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 and Down syndrome Down syndrome, congenital disorder characterized by mild to severe mental retardation, slow physical development, and characteristic physical features. Down syndrome affects about 1 in every 730 live births and occurs in all populations equally.
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. The sex of the child can also be ascertained. Although CVS tests for the same range of abnormalities as amniocentesis amniocentesis , diagnostic procedure in which a sample of the amniotic fluid surrounding a fetus is removed from the uterus by means of a fine needle inserted through the abdomen of the pregnant woman (see pregnancy).
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, it is usually performed some weeks earlier (between the 8th and 12th weeks of pregnancy), and the results are available in a few days. It is recommended if the parents are carriers of certain genetic diseases, if there is a family history of genetic disorders, or if the woman is over age 35 (later pregnancies carrying with them a higher risk of chromosomal abnormality).
chorionic villus sampling [¦kör·ē‚an·ik ′vil·əs ‚sam·pliŋ]
(medicine)
A technique in which samples of chorionic villi are taken from the placenta for the purpose of genetic testing; usually performed at the end of the second month of pregnancy.


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When using a chorionic villi sampling, the process is conducted during the 10th through the 13th week of pregnancy.
3) Options for carrier couples Carrier couples may elect to have preimplantation genetic analysis in order to assure an unaffected pregnancy, or prenatal diagnosis using chorionic villi sampling (CVS) in the first trimester, or amniocentesis in the second trimester.
The procedure, chorionic villi sampling (CVS), has been used in the past 10 years at prenatal diagnostic centers, including hospitals, outpatient clinics and obstetricians' offices.
 
 
 
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