The triple screening test is recommended by many specialist doctors during pregnancy and congenital diseases such as some chromosomal abnormalities and neural tube defects in the baby are investigated. During pregnancy, the health of the mother and baby is very important.
Nowadays, many tests are performed for mothers during pregnancy to keep maternal and infant health under control. The tests performed are performed at certain December intervals and at certain periods.
16 of pregnancy. and 20. the triple screening test performed during the week December is a more comprehensive test compared to the double screening test performed earlier. The triple screening test is very important in terms of maternal and infant health and is one of the tests that every mother should have.
A triple screening test is one of the tests performed to screen for certain diseases and provides a lot of information about pregnancy. Specialist obstetricians and gynecologists require mothers to take certain tests during certain periods of pregnancy.
Double and triple screening tests performed in the early stages of pregnancy are used to screen for genetic diseases called Down syndrome, trisomy 18. The triple screening test is a very easy and comfortable procedure.
A triple screening test is also recommended for pregnant women in cases where some anomalies are observed by obstetricians or who do not carry any risk. Some blood is taken from the mother’s arm for a triple screening test.
The blood taken is sent to special laboratories and evaluated by specialists and turned into a report. In order for the accuracy value of the test to increase, detailed research should be carried out at the appropriate time and by expert persons.
According to the result of the test, expectant mothers may also be requested to have different tests in order to get a final result. It allows the triple screening test to obtain results only on chromosomal abnormalities that occur on the baby’s chromosomes. With this test, the baby’s intelligence is not measured.
16 of pregnancy. and 20. between the first week with a screening test that is performed during pregnancy, the baby may be in some chromosomal abnormalities, neural tube defects called congenital diseases is a test that is performed to investigate.
Babies get half of the 46 chromosomes from the mother and half from the father. However, in some cases, some problems may occur in the chromosome sequences. The risks related to chromosomal abnormalities occurring in infants are determined with the double-triple scans performed.
Unlike the double screening test, it is possible to use the triple test to investigate congenital anomalies called neural tube defects. If there is a high probability of some chromosomal abnormalities in the baby with a triple screening test, CVS or amniocentesis can be performed for people. Trisomy18 is a condition that causes mental retardation in the baby and diseases related to anomalies in many other organs.
The triple screening test, which investigates the possibility of trisomy 21, trisomy 18 and neural tube defects during pregnancy, is important in terms of preventing some diseases that occur.
According to the results of the tests, trisomy 21, that is, downsyndrome, causes some physical problems and mental retardation in the baby. Trisomy 21 is a condition that occurs due to the fact that chromosome 21 has 3 pieces, while it should have 2 pieces.
Another disease that is being investigated after the triple screening test is trisomy 18, aka Edward’s syndrome. Trisomy 18 is a condition that occurs due to the fact that 18 chromosomes are 3 when they should be 2. Babies with these conditions are unlikely to live in the womb or after birth.
The problems of neural tube defects investigated by triple scanning are the formation of brain tissue that does not develop in the baby. The results reported as a result of the examination of the blood taken from the mother in laboratory settings are,
it should be interpreted by a specialist obstetrician and families should be informed. Triple screening tests only indicate the risk status by investigating the possibility of encountering diseases.
during the 40-week pregnancy period, mother and baby health is a very important consideration. During this long pregnancy process, the mother needs to be in constant communication with a specialist obstetrician-gynecologist and take the recommended tests.
16 of pregnancy. and 20. between the weeks, mothers are indicated that triple screening tests should be performed by specialist doctors. Dec. Triple screening tests are 15 due to some conditions. and 22. it can also be done between weeks Dec. A double screening test is performed before the triple screening test.
After the double screening test, a triple screening test is needed to detect chromosomanomalies that may occur in the baby. With triple screening tests, it will become even clearer to detect genetic disorders such as Down syndrome and Edward syndrome.
For this reason, mothers who have had a double screening test by doctors are also advised to have a triple screening test. A triple screening test is a fairly simple procedure performed with a small amount of blood taken from the mother. Triple screening tests do not have any risk factors for maternal and infant health.
16 of pregnancy. and 22. it does not matter if the mother is hungry or full for the triple screening test performed between the weeks Dec. The triple screening test can be performed easily at any time of the day when the mother is hungry or full. In the triple screening test performed, the risk ratio is determined by taking into account details such as the mother’s weight, age, whether she smokes or not.
The important thing in the triple screening test is that the ultrasound is performed on the same day as the blood donation procedure, a lot changes in the body within 1 day during pregnancy. It is not possible to definitively detect Down syndrome or other chromosomal abnormalities with triple screening and double screening tests, which are recommended for all pregnant pregnant women.
During pregnancy, a triple screening test is performed to investigate chromosomal disorders. Risk situations are investigated after triple screening tests. People who are at risk as a result of triple screening tests are given some tests again later. The results of triple screening tests performed usually show a high risk of a baby with downsyndrome.
In the researches carried out, after triple screening, the detection rate of children who will be born with downsyndrome in many people is 60-65%. In order to make a definitive diagnosis in screening tests, people may need to undergo tests such as CVS and amniocentesis later.
The result of triple screening tests should not be evaluated. When evaluating the results of triple screening tests, factors such as the mother’s age, body weight, diabetic status, smoking consumption should be taken into account.
Normal values of triple screening tests are considered to be the limit value for Down syndrome, 1/250. The results above this value are interpreted as positive.
The limit value for Edward’s syndrome is considered to be 1/100. Test results above this value are interpreted as positive. It is of great importance to carry out the necessary tests in time to eliminate the risks that may occur in cases above all these limit values.
Triple screening test prices may differ depending on the institution where the procedure will be performed and where the institution is located. Triple screening tests are tests that can be performed in private hospitals and public hospitals.
The evaluation of the blood results examined in the laboratory environment should be carried out by specialists and experienced people. Ignoring the gestational week, weight and some pregnancy values in triple screening tests are restrictive factors in terms of evaluating the result. Dec.
For triple screening test prices, it is necessary to contact the healthcare provider where the procedure will be performed. Contact us immediately to get information about triple screening test prices 2024.
