My wife is 12.4 weeks pregnant, when NIPT test, chromosomes 21, 18, 13 are normal but Monosomy X 9%. So I would like to ask the doctor, Doctor, is the NIPT Monosomy X 9% test result during pregnancy okay? Will the fetus develop normally, will the child be born with genetic problems and what is the most accurate method? My wife was born in 1982, this is her second birth. Thank you.

Pregnant women are only offered amniocentesis when absolutely necessary. For pregnant women carrying twins, amniocentesis requires taking samples from two separate amniotic sacs. This leads to a higher risk of complications than in singleton pregnancies.

Amniocentesis is a procedure used for prenatal diagnosis after a doctor detects an abnormality in the fetus's chromosomes. So how is amniocentesis performed and what precautions should pregnant women take before having an amniocentesis test?

Genetic disorders are caused by genes called mutations. Genetic disorders include sickle cell anemia, cystic fibrosis, Tay-Sachs disease, and many more. Most cases of these disorders occur when both parents carry the same abnormal gene.

Many babies with hemolytic disease whose parents did not screen them for the disease before birth require blood transfusions and treatment for most of their lives. Some babies with the disease only live a few years.

By age 40, the chances of getting pregnant are lower, but many women in this age group still conceive naturally or use assisted reproductive techniques. Every age has its advantages and disadvantages when it comes to getting pregnant.

Patau syndrome is one of the chromosomal abnormalities encountered in the fetus, causing the baby to die in the womb or after the first year of life. NIPT screening helps detect Patau syndrome early.

Many people think that the age of 30 is the best time to be a mother, because at this time the job, income, and relationships have become stable. But in fact, being a mother at different ages will have different advantages and disadvantages.

Patau Syndrome - One of the most common genetic syndromes in fetuses, like other congenital malformation syndromes, Patau syndrome seriously affects the health of children from the time they are in the womb.

The first trimester (first 3 months of pregnancy) is the time to conduct prenatal screening to detect certain genetic disorders in the baby early, especially Down syndrome (trisomy 21) and trisomy 18.

Children with Down syndrome often reach developmental milestones a little later than their peers. If you have had one child with Down syndrome, your risk of having a second child with Down syndrome is slightly increased.