For Amniocentesis we have terms and definitions in 18 topics. The topics are Anthromorphemics, Anthropology, Baby, Female Health, Fertility, Genetics, Health, Human Reproduction, Huntingtons Disease, Invitro Fertilization, Medical, Pompe Disease, Prader-Willi Syndrome, Pregnancy, Science, Sex, Women's Health and Womens Health.

Amniocentesis (Anthromorphemics)

A medical technique in which amniotic fluid is removed for study of the fetus.

Amniocentesis (Anthropology)

A medical technique in which amniotic fluid is removed for study of the fetus.

Amniocentesis (Baby)

A test to determine possible obstetric complications or genetic defects usually performed between the 15th and 18th weeks of pregnancy. Amniotic fluid is drawn from a pregnant woman's uterus by inserting a hollow needle through her abdominal wall.

Amniocentesis (Female Health)

This test is performed between the 14th and 18th week of pregnancy. Essentially, this test will enable your healthcare professional to look at fetal cells in the amniotic fluid for signs of certain birth defects. A normal result does not guarantee the birth of a normal baby. During this diagnostic procedure, a needle is inserted into the amniotic sac and a small amount of fluid is removed. If you are 35 or older at the time of delivery, there's a good chance your healthcare professional will recommend this test because women over 35 have a higher risk of having a baby with Down's syndrome. It's also recommended if you've already had a child with a birth defect, or if you have a family or personal history that puts you at risk for an inherited disease.

Amniocentesis (Fertility)

Test performed between the 16th and 18th week of pregnancy in order to determine the presence of birth defects in the developing fetus. It involves the insertion of a small needle into the amniotic fluid that surrounds the developing baby. The fluid is then screened for genetic conditions such as Down Syndrome

Amniocentesis (Genetics)

Prenatal diagnosis method using cells in the amniotic fluid to determine the number and kind of chromosomes of the fetus and, when indicated, perform biochemical studies.

Amniocentesis (Health)

A test performed to determine chromosomal and genetic disorders and certain birth defects. The test involves inserting a needle through the abdominal and uterine wall into the amniotic sac to retrieve a sample of amniotic fluid.

Amniocentesis (Human Reproduction)

Aspiration of amniotic fluid, usually transabdominally, for diagnostic or therapeutic purposes.

Amniocentesis (Huntingtons Disease)

A medical procedure in which cells from the fetus are obtained from the fluid within the innermost fetal membrane.

Amniocentesis (Invitro Fertilization)

A procedure which is usually carried out at around 15-16 weeks of pregnancy. It involves aspirating a small amount of the fluid which surround the baby in the womb. This fluid contains cells from the baby which can then be cultured and tested to determine the baby's chromosome. The procedure is usually performed under ultrasound scan using a fine needle. The risk of causing miscarriage by this procedure is between 0.5 - 1%. The results often take two to three weeks.

Amniocentesis (Medical)

A procedure in which a small amount of amniotic fluid is removed from the mother’s womb in order to detect abnormalities of the fetus

Amniocentesis (Pompe Disease)

Withdrawal of fluid from the amniotic sac, the innermost membrane surrounding the fetus containing amniotic fluid.

Amniocentesis (Prader-Willi Syndrome)

A procedure in which a small amount of the amniotic fluid surrounding the fetus is drawn off and subjected to genetic and biochemical analysis.

Amniocentesis (Pregnancy)

Amniocentesis is a test used to detect various genetic defects or lung maturity of an unborn baby by using a needle to remove a small amount of fluid from the amniotic sac surrounding the baby.

Amniocentesis (Science)

A method for detecting genetic diseases in unborn babies. A needle is inserted through the mother's abdomen to remove fluid from the sac surrounding the fetus in the mother's womb; the fluid and the cells in the fluid can be examined to see if the baby will have a genetic disorder.

Amniocentesis (Sex)

A diagnostic procedure in which amniotic fluid is withdrawn by needle from the uterus of a pregnant woman. The fluid and fetal cells are then analyzed for chromosome defects.

Amniocentesis (Women's Health)

If necessary, this test is performed between 15 and 20 weeks of pregnancy and can indicate chromosomal abnormalities such as Down syndrome, or genetic disorders such as Tay Sachs disease, sickle cell disease, cystic fibrosis, and others. It also can detect the baby's sex and risk of spina bifida (a condition in which the brain or spine do not develop properly).

Amniocentesis (Womens Health)

If necessary, this test is performed between 15 and 20 weeks of pregnancy and can indicate chromosomal abnormalities such as Down syndrome, or genetic disorders such as Tay Sachs disease, sickle cell disease, cystic fibrosis, and others. It also can detect the baby's sex and risk of spina bifida (a condition in which the brain or spine do not develop properly).

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