You may also need an amniocentesis if your doctor suspects that your unborn child has an infection or anemia.
Women who have had a previous child with a birth defect, a family history of genetic conditions like cystic fibrosisor who have suspicious results on other screening tests blood tests for neural tube defects, for example will probably also get the test. Anencephaly when the baby is missing a large portion of the brain Down syndrome Rare metabolic disorders that are passed down through families Other genetic problems, like trisomy 18 Infections in the amniotic fluid Normal Results No genetic or chromosome problems were found in your baby.
If this happens, your doctor will give you a drug called RhoGAM. After the risks and benefits of amniocentesis have been thoroughly explained to you, you can choose whether or not you want to have the procedure. The test results can help you determine whether to continue with your pregnancy.
She seems sure of the health of her baby in these two lines.
The risk of miscarriage is 0. Her imagery suggests that throughout the poem. Amniocentesis can identify these abnormalities. The first one is in the first line of the poem: This helps your health care provider see where the baby is in your womb.
This is a difficult time for parents, so seek support from your loved ones, your doctor, or a support group. What Are the Complications Associated with Amniocentesis? You do not need to stay in the hospital. How Accurate Is Amniocentesis?
Johnson, MD on June 07, Sources. You will have a pregnancy ultrasound first. A small amount of fluid about 4 teaspoons or 20 milliliters is removed from the sac surrounding the baby. The fluid contains cells that your baby has sloughed off, plus chemicals and microorganisms.
Amniotic fluid surrounds your unborn baby. After Amniocentesis essay amniocentesis, it is best to go Amniocentesis essay and relax for the remainder of the day. Genetic studies Measurement of alpha-fetoprotein AFP levels a substance produced in the liver of the developing baby Culture for infection Results of genetic testing usually take about 2 weeks.
Under ultrasound guidance, the doctor inserts a thin, hollow needle through your abdomen and uterus, and into the amniotic sac, away from the baby. Artificial heart valves, working tracheas, as well as muscle, fat, bone, heart, neural and liver cells have all been engineered through use of amniotic stem cells [ citation needed ].
The fluid is sent to a laboratory. If you or your partner is a known carrier of a genetic disorder, such as cystic fibrosis, amniocentesis can detect whether your unborn child has this disorder.Amniocentesis is where a procedure is done to remove fluid from the amniotic sac.
The amniotic sac is the fluid that is inside the uterus. The amniocentesis procedure is done by injection a long needle through the abdominal and the uterine wall into the amniotic sac.
Note: Amniocentesis typically is the most accurate test for genetic conditions and malformation, Although rare, a baby may still have genetic or other types of birth defects, even if amniocentesis results are normal. Amniocentesis is a diagnostic test that may be recommended by your health care provider.
Genetic concerns lead some parents to choose amniocentesis. Amniocentesis is a procedure in which your doctor removes a small amount of amniotic fluid from your womb to test for genetic abnormalities. amniocentesis Essays: Overamniocentesis Essays, amniocentesis Term Papers, amniocentesis Research Paper, Book Reports.
ESSAYS, term and research papers available for UNLIMITED access. Amniocentesis (also referred to as amniotic fluid test or AFT) is a medical procedure used in prenatal diagnosis of chromosomal abnormalities and fetal infections.Download