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Topic: NIPT screening for baby chromosomes For the strength of the children in the future

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NIPT screening for baby chromosomes For the strength of the children in the future
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ตรวจ NIPT คัดกรองโครโมโซมลูกน้อย เพื่อความแข็งแรงของเด็กในอนาคต

 

 

What is a NIPT test?

Dr. Naphawaree Chantawong, MD, specialized in obstetrics and gynecology World Medical Hospital (WMC) states that NIPT or Non-Invasive Prenatal Testing is a screening for fetal chromosomal abnormalities from the mother's blood. Can find the risk of developing สล็อต xo ทดลองเล่นฟรี Down syndrome or another important chromosomal abnormality Including the sex chromosome of the fetus This method greatly reduces the risk to the fetus. Because they do not want to penetrate the amniotic fluid Thus making it safe for mothers and fetuses, as well as being highly accurate

Usually, humans have a total of 23 chromosomes, or 46 chromosomes (mother, 23, paternal, 23 chromosome). Chromosomal abnormalities can occur in a number of ways, such as having one extra chromosome, one missing, or missing. To some part of the chromosome

 

Advantages of a NIPT test

Fast and convenient

 

 

• Very high accuracy, up to 99%.

100% safe

• able to detect multiple chromosome pairs Cover various disease risks

Know the gender of the baby Can be from 10 weeks gestation

 

Which mothers should be examined?

• The age of 30 years as the risk of developing disease increases with the age of pregnant women.

• having a family history of family and kinship with a genetic disease

• The fetus comes from in vitro fertilization.

IVF Or have a history of miscarriages

• People who cannot detect chromosomal abnormalities from amniocentesis or placental biopsy.

• All pregnant women can be examined.

 

However, chromosomal abnormalities can be caused by a number of reasons. Some are independent of the age of the mother. But it can be caused by inheritance, chemical, or a combination of reasons. Should be consulted by a medical professional



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