Down syndrome, also known as Down syndrome, is the most common birth defect in children caused by autosomal abnormalities. As the name suggests, this disease is an intelligent disorder with a specific phenotype caused by congenital factors. So, how to diagnose Down syndrome?
If Down syndrome is diagnosed during fetal development, we believe there are two aspects to consider. Firstly, if the screening is high-risk, blood tests or B-ultrasound are usually performed. If any abnormalities are found, we will perform chorionic villi puncture, amniocentesis or umbilical cord blood puncture. By taking fetal cells for core analysis, we can confirm whether it is Down syndrome, which is the gold standard.
Another diagnostic method is not to do Down syndrome screening. If the child is older or has previously had Down syndrome, they may not undergo screening if they become pregnant again. It is recommended to draw amniotic fluid, perform umbilical cord blood puncture, early pregnancy chorionic villi puncture, and perform core analysis of the fetus. The main diagnostic method is to check whether the fetus has Down syndrome through core analysis.
Early parenting care is necessary for patients with Down syndrome, as it helps with their development. The treatment mainly involves intelligent training, exercise of motor function, and prevention of complications. Firstly, it is possible to accurately diagnose the symptoms of Down syndrome, comprehensively analyze its causes, and regulate children with intellectual disabilities and language disorders as a whole. Then, corresponding treatment plans can be developed for different stages of the treatment process based on the symptoms.
