Genetics & New
Born babies
Photo by Sunvani Hoà ng: https://www.pexels.com/photo/happy-asian-girl-child-embracing-newborn-baby-lying-on-bed-7973597/
There are wide range of factors which can lead to lifelong
disability in children. The factors
include illness, injury, environmental factors, socio-economic while Genetic also
play a crucial role in development of a baby.
Certain genetic conditions can lead to disabilities that can impact
a child's life significantly. Genes are the instructions that determine an
individual's physical and biological characteristics, including susceptibility
to certain diseases and conditions.
When a baby is born, they
inherit half of their genes from their biological mother and half from their
biological father. Genetic disorders are caused by changes or mutations in the
DNA sequence of genes, which can affect the way a person's body functions. Some
of these mutations can lead to physical or intellectual disabilities that can
be present from birth or may develop later in life. Therefore, the health of a baby can be influenced by the genetic makeup
of their parents. If one or both parents have a genetic predisposition to a
particular disease or condition, their child may be more likely to develop it
as well. For example, if a parent has a family history of heart disease or
diabetes, their child may have an increased risk of developing these
conditions.
Some genetic conditions are present at birth, while others may not become apparent until later in childhood. However, it's important to note that genetics is not the only factor that determines a baby's health. Environmental factors, such as diet, lifestyle, and exposure to toxins, can also play a significant role. Additionally, advances in medical technology and healthcare can help identify and manage health conditions in newborns.
By understanding the causes of disability in children, we can work
towards creating a more inclusive and accessible society for all children,
regardless of their abilities.
