Analysis of Down Syndrome Risk Rate

The risk value for Down syndrome 21-trisomy during pregnancy is 1 in 651, it is recommended to undergo further tests such as non-invasive DNA testing or amniocentesis.

Both NT screening and trisomy screening are important tests for understanding the health of the fetus.

Elderly pregnant woman, four-dimensional scan normal, genetic chip test shows a deletion in the short arm of chromosome 10, can the fetus be preserved?

Can a fetus suspected of having hydrocephalus exhibit movements?

Currently, amniocentesis can only detect chromosomal abnormalities and neural tube defects; it cannot detect genetic metabolic diseases. Genetic metabolic diseases can have serious impacts on a child’s health and require timely and accurate treatment.

Can parents with Type A and B blood types have a child with Type O?

Consultation on amniocentesis for genetic metabolic disorders

Methods for diagnosing and preventing phenylketonuria

An umbilical cord cyst during pregnancy may be associated with fetal chromosomal abnormalities. Amniocentesis is a method for further diagnosis, although it carries a risk of miscarriage, the risk is relatively low under the operation of a regular hospital.