Early Detection After Birth Protects Infants from Serious Genetic Disorders

Newborns and Mothers.

The Ministry of Health and Population has emphasized that just one minute after birth can mark a critical point in protecting infants from complications associated with genetic disorders. This can be achieved through necessary screenings for early detection of hereditary diseases in newborns.

The ministry explained that metabolic disorders are among the genetic diseases caused by enzyme deficiencies that affect the digestion and metabolism of food within the body. Early diagnosis allows for prompt medical intervention, which contributes to improving the quality of life for children and reducing potential health complications.

Furthermore, the state provides free screening and treatment services for these conditions as part of the presidential initiative for early detection of genetic disorders in newborns, ensuring that essential healthcare is available to children from their very first days.

The ministry stressed the importance of early detection as a fundamental step towards building a healthier future for children, enhancing their opportunities for normal and safe growth and life.