Who is Prone to Chromosomal Abnormalities?

Diagnosis of interchromosomal translocation on chromosome 9 (iv(9)(p12q13)) and its potential effects on fertility and fetal development.

The baby has a broken palm on both hands, and the risk of Down syndrome screening during pregnancy was high. The low-risk result of non-invasive DNA testing suggests that the baby is unlikely to have Down syndrome.

Understanding a Baby’s Growth Status and Its Influencing Factors

A fetal 21 chromosome anomaly may be caused by a genetic mutation, not necessarily inherited from the parents.

The prognosis of bile duct obstruction depends on its type and the timing of treatment. Infections, genetic mutations, immune factors, and exposure to harmful substances during pregnancy can all lead to bile duct obstruction in children. However, paying close attention to these factors can effectively prevent bile duct obstruction. Additionally, newborns and infants should be screened early for obstructive jaundice to enable early diagnosis and treatment.

Explore the causes of cerebral palsy in children, including genetic and acquired factors, and provide professional medical advice.

Exploring the Relationship Between Congenital Preauricular Sinus and Genetic Factors

Down syndrome screening is a method to check if a fetus has Down syndrome, which is related to the age of the pregnant woman.

Whether dwarfism is genetic depends on the genes.