Prenatal Screening Program
The program’s objective is the timely diagnosis of chromosomal abnormalities in the foetus and is offered to all women in their first trimester of pregnancy.
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The program’s objective is the timely diagnosis of chromosomal abnormalities in the foetus and is offered to all women in their first trimester of pregnancy.
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All neonates undergo screening tests for congenital hypothyroidism and phenylketonuria (PKU) once they have fulfilled their first 48 hours of life. These metabolic diseases can lead to very severe and irreversible health problems unless the affected child is promptly placed on therapy following early diagnosis.
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The aim of the Program is the timely detection and diagnosis of congenital hearing loss in newborns, since hearing is crucial for the development of speech, learning, and social integration. Early intervention helps prevent communication difficulties and poor school performance.
Learn moreBy making your contribution, you help support the continuation of our work. Because every child has the right to a healthy start!
28-10-2025
23-10-2025
17-09-2025