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How long does it take to get the results from a amniotic fluid test?
Wiki User
∙ 12y ago
Five years.
Wiki User
∙ 12y ago
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What is a amniocentesiss?
Its a medical procedure where they take a small amount of fluid from around the fetus, the fluid is called amniotic fluid. Then this is tested for any chromosome abnormalities, so they can check if the child will have any sever genetic problems, because the amniotic fluid contains fetal tissues which contains chromosomes.
What is the cell culture of the amniotic fluid in a woman's womb?
Under guidance of ultrasonography machine you take the amniotic fluid sample. This is usually done after 12 weeks of gestation to avoid injury to fetus. Cells there in, are harvested and cultured. They give you complete genetic information of the fetus.
How is amniocentesis carried out?
A needle through your stomach to take a sample of the amniotic fluid, very painful and is very dangerous for baby as has a high chance of causing miscarriages.
Do you have to wait until baby is born to do paternity test?
No, you can undergo procedures such as amniocentesis that take some of the foetus' cells that are discarded into the amniotic fluid surrounding it, that will contain its DNA.
What is used to tell what an offspring will turn out to be?
If the doctor can see a sex organ on the fetus using ultrasound, then that is a good way to tell. Otherwise, they can take a sample of amniotic fluid that surround the fetus, using a needle, then testing the fluid for male or female.
What are aminocentesis?
Amniocentesis (also referred to as amniotic fluid test or AFT), is a medical procedure used in prenatal diagnosis of genetic risk factors, in which a small amount of amniotic fluid, which contains fetal tissues, is extracted from the amnion or amniotic sac surrounding a developing fetus, and the fetal DNA is examined for genetic abnormalities.Before the actual procedure, a local anesthetic is sometimes given to relieve the pain when inserting the syringe to withdraw the fluid. A syringe is usually inserted through the mother's abdominal wall or at the end of the vagina, and through the wall of the uterus into the amniotic sac. With assistance from ultrasound a physician aims an area of the sac that is away from the fetus and extracts a small amount of amniotic fluid for testing. The puncture heals, and the amniotic sac automatically replenishes the liquid over a day or so. After the amniotic fluid is extracted, the fetal cells are separated from it using a centrifuge, and cell chromosomes are examined for abnormalities. Various genetic testing may be performed, but the three most common abnormalities tested for are Down's syndrome, Trisomy 18 and spina bifida. Amniocentesis can be performed as soon as sufficient amniotic fluid surrounds the fetus to allow a sample to be recovered relatively safely, usually no earlier than the 14th week of pregnancy. Often, genetic counseling is offered in conjunction with amniocentesis.
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