Discussing the Genetic Risk and Prevention Measures of Mental Illness

The Down syndrome screening indicates a high risk of Trisomy 21 syndrome. How should one consider the issue of fetal retention?

Embryos or fetuses with chromosomal abnormalities usually result in spontaneous abortion, and it is recommended to use in vitro fertilization for assistance in conception.

Patients with chromosomal abnormalities inquire about the possibility of having a healthy baby through in vitro fertilization (IVF) technology.

Hemophilia cannot be cured at present, and is primarily managed through medication and the supplementation of coagulation factors for prevention and treatment. Patients should avoid injuries and refrain from using drugs that dilate blood vessels or inhibit platelet aggregation. Additionally, genetic counseling should be provided for both the patient and their family.

Roberts’ Syndrome Patient Inquires About the Possibility of Having a Healthy Child and Suggestions

Inquire about the possibility of genetic inheritance of intellectual disability and how to confirm it through hospital examinations.

Chromosomal abnormalities in the embryo may be due to issues with the parents’ chromosomes or problems during the delivery process. If both parents have normal chromosomes, there is still a possibility of a normal pregnancy. It is recommended to undergo checks and maintain a regular lifestyle.

Congenital chromosome abnormalities may be inherited across generations. It is recommended to undergo chromosome testing, pay attention to lifestyle habits, and provide children with enough care and attention.

The risk of Down syndrome is 1 in 812, the risk of trisomy 18 is 1 in 42,321, and the risk of an open neural tube defect is 1.07. Do you need to undergo non-invasive prenatal testing (NIPT)?