What does Down Syndrome check, and what benefits does it have for pregnant women and fetal development?

Down Syndrome is a congenital mental retardation caused by a chromosomal abnormality. Infants born with Down Syndrome are referred to as Down’s babies. This is a congenital defect, with infants experiencing intellectual disability after birth, often accompanied by congenital heart disease and poor self-care abilities. These conditions can be detected early during pregnancy through Down Syndrome screening, Non-invasive Prenatal Testing (NIPT), or amniocentesis.

A detailed explanation of Down syndrome and its corresponding clinical features.

Down syndrome is a genetic disorder that typically occurs during fetal development, characterized by an extra 21st chromosome in the body’s cells.

Down syndrome is a genetic disorder caused by trisomy of the 21st pair of chromosomes. Symptoms include delayed intellectual development and specific physical characteristics. There is no cure at present, but it can be detected through prenatal tests in the early stages of pregnancy.

Down syndrome is a genetic disorder characterized by intellectual disability and specific physical abnormalities. Symptoms may include distinctive facial features, developmental delays, heart problems, and more.

Facial palsy, also known as Bell’s palsy, is an idiopathic, acute onset unilateral peripheral facial nerve paralysis.

Facial paralysis occurs when the facial nerves are attacked by cold winds, leading to severe pain in the microvessels, which causes regional tissue brain edema and swelling.

Facial paralysis is a disease that affects the facial nerve, with main symptoms including the disappearance of forehead lines, inability to furrow the brows, incomplete closure of the eyelids, and drooping of the corners of the mouth.

The main symptoms of facial paralysis include mouth distortion incline, drooling, and abnormal facial muscle activity.