How do Genomic Variations Affect Neonatal Disorders?
Genomic variations can lead to a wide range of neonatal disorders, from metabolic issues to structural abnormalities. For instance, a mutation in a single gene can cause conditions like cystic fibrosis or sickle cell anemia. On the other hand, chromosomal abnormalities such as trisomy 21 result in Down syndrome. These variations can affect the development, health, and survival of newborns.
