Chorionic Sentence Examples

The embryo passes through three stages - (I) still enclosed within the egg and living on its own yolk; (2) free, within the vitelline mass, which is directly swallowed by the mouth; (3) there is no more vitelline mass, but the embryo is possessed of long external gills, which serve for an exchange of nutritive fluid through the maternal uterus, these gills functioning in the same way as the chorionic villi of the mammalian egg.

A urine test will detect human chorionic gonadotropin (HCG) which.. .

This risk is slightly higher with chorionic villus sampling.

Diagnostic tests Chorionic villus sampling This means taking a sample of a piece of tissue from the placenta.

Maternal blood samples were collected at prior to chorionic villous sampling.

Please avoid sending chorionic villus samples on a Friday.

In general, a 10 ml sample of amniotic fluid or a chorionic villus biopsy is required.

Procedures such as amniocentesis or chorionic villus sampling allow small amounts of the baby's cells to be removed for examination.

This can be done after ten to 12 weeks of pregnancy using a procedure called chorionic villus sampling (CVS).

This was followed by the development of two natural hormones, follicle-stimulating hormone and chorionic gonadotrophin (Pergonal) to produce multiple eggs ovulation.

A chorionic villus sampling test during the fifth week of pregnancy may also reveal some types of albinism.

Prenatal diagnosis of types A and B NPD can be done with amniocentesis or chorionic villi sampling.

Amniocentesis or chorionic villi sampling can be used to determine if the fetus has Tay-Sachs disease.

During pregnancy, cell samples can be collected from the fetus using amniocentesis or chorionic villi sampling.

This can be accomplished using procedures such as an amniocentesis or chorionic villus sampling (CVS), after which parents can explore their options relating to the pregnancy.

When a woman is already pregnant, tests can be performed on either the cells of the fetus (amniocentesis) or the placenta (chorionic villus sampling) to determine whether the baby will have Tay-Sachs disease.

Since additional congenital defects preclude prenatal surgery, amniocentesis or chorionic villi sampling (CVS) are used to check for chromosomal abnormalities in the fetus.

Chorionic villus sampling-A procedure used for prenatal diagnosis at 10-12 weeks gestation.

Under ultrasound guidance a needle is inserted either through the mother's vagina or abdominal wall and a sample of the chorionic membrane.

As of the early 2000s it has been shown that biochemical diagnosis can be performed through chorionic villus testing, a procedure performed very early in the first trimester of pregnancy.

An amniocentesis or chorionic villus sampling can be used to obtain fetal cells which can be analyzed for the RB1 gene change/deletion or chromosomal abnormality.

Genetic testing for and detection of the fragile X mutation can be performed on the developing baby before birth through amniocentesis, chorionic villus sampling (CVS), and percutaneous umbilical blood sampling.

The chorionic membrane can be examined for signs of chromosome abnormalities or other genetic diseases.

Chorionic villus sampling (CVS) can be done as early as 10 weeks of pregnancy.

Patau syndrome is detectable during pregnancy through the use of ultrasound imaging, amniocentesis, and chorionic villus sampling (CVS).

Chorionic villus sampling is a procedure that obtains a sampling of cells from the placenta for testing.

Chorionic villus sampling can be performed at ten to 12 weeks of pregnancy.

Testing can be done at 10-12 weeks gestation by a procedure called chorionic villus sampling (CVS) that involves removing a tiny piece of the placenta and analyzing DNA from its cells.

An alternative to amnio, now in general use, is chorionic villus sampling, or CVS, which can be performed as early as the eighth week of pregnancy.

Chorionic villous sampling is a test that examines proteins for deficiencies or defects that are characteristic of hemophilia.

Potential tests include maternal serum alpha-fetal protein analysis or screening, ultrasonography, amniocentesis, and chorionic villus sampling.

This test is not a definitive indicator of a problem and is followed by more specific testing such as amniocentesis or chorionic villus sampling.

This can be done in pregnancy with prenatal testing such as chorionic villus sampling or amniocentesis.

Chorionic villus sampling is a procedure done early in pregnancy (approximately 10-12 weeks) to obtain a small sample of the placenta for testing.

Cri du chat syndrome can be detected before birth if the mother undergoes amniocentesis testing or chorionic villus sampling (CVS).

Specialized testing of chromosome 15 will be required; the usual tests done during amniocentesis or chorionic villi sampling will not reveal the specific, small genetic flaw that causes Angelman syndrome.

Chorionic villus sampling (CVS) is a procedure that allows for prenatal diagnosis during the first trimester (generally between ten and 12 weeks of gestation, during the embryonic stage of development).

Then, early in a pregnancy, cells can be obtained from the developing fetus by chorionic villus sampling or amniocentesis and checked for the same mutation.

Rhogam should also be given after any episode of bleeding and after amniocentesis or chorionic villus sampling.

This is usually done either by amniocentesis or chorionic villus sampling (CVS).

It is up to 99 percent accurate from the first day of your missed period, provided you have detectable amounts of human chorionic gonadotropin (hCG) in your urine.

The test detects the level of human chorionic gonadotropin (HCG) in the urine, which is only produced during pregnancy.

The First Response Pregnancy Test is designed to test the level of human chorionic gonadotropin (hCG) in your urine.

All pregnancy tests look for the presence of hCG, or human chorionic gonadotropin.

A blood test for the pregnancy hormone human chorionic gonadotropin (HGC) will probably be abnormal.

Pregnancy tests look for a hormone called human chorionic gonadotropin (HCG), which is associated with pregnancy.

A home pregnancy test works to detect a hormone in the blood called Human Chorionic Gonadotropin (HCG).

Pregnancy tests look for a pregnancy hormone called human chorionic gonadotropin (HCG).

Blood tests may be run to check for a normal level of human chorionic gonadotropin (hCG), a pregnancy hormone that rises with pregnancy.

First Response has created a test that can detect lower levels of the hormone hCG (human chorionic gonadotropin), also known as the pregnancy hormone.

After conception, the pregnancy hormone hCG (Human Chorionic Gonadotropin) secretes from the developing placenta after the egg implants in the uterine lining.

The purpose of a home pregnancy test is to check your urine for the presence of human chorionic gonadotropin (HcG).

Depending on your answers to these questions, your provider may recommend further testing, such as Chorionic Villus Sampling or a First Trimester Screen.

When the joined sperm and egg implant into the womb, the human chorionic gonadotropin (hCG) is produced.

Pregnancy tests work by measuring levels of the pregnancy hormone, human chorionic gonadotropin (hCG) in your urine or blood.

If you picked a test with a low sensitivity and your period is only a few days late, you may not be producing enough human chorionic gonadotropin (hCG) to trigger a positive result.

The test measures levels of the pregnancy hormone, human chorionic gonadotropin (hCG) in your urine.

It is the implantation in the uterus that causes the release of human chorionic gonadotropin (hCG), the hormone of pregnancy.