Treatment and Causes of Down Syndrome
Inquiring about treatment options for fetal chromosome abnormalities and whether to attempt a second pregnancy
A three-month-old boy is found to have accessory breasts, and inquiries are made about the possibility and impact of genetics.
This article discusses the causes, diagnosis, and preventive measures for embryonic chromosomal abnormalities.
How to treat hyperuricemia in newborns and conduct relevant tests
Information on the treatment of dwarfism and genetic factors
Treatment for chromosomal abnormalities is limited, it is recommended to enhance nutrition and undergo rehabilitation therapy to help patients live as independently as possible.
A two-and-a-half-year-old girl was born with jaundice and is suspected of having her growth affected. The doctor provided nutrition and trace element recommendations.
Chromosomes are the carriers of genetic information, located within the cell nucleus, and are an important foundation of human genetics.
This article introduces approximately 3,000 genetic diseases in the world, including dominant and recessive chromosomal diseases, X-linked genetic diseases, polygenic genetic diseases, and chromosomal disorders.