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The NHS will screen all newborns for a deadly genetic disorder to enable early treatment and better outcomes.
The NHS will begin screening all newborns for a life-threatening genetic disorder, aiming to detect early symptoms such as feeding difficulties, poor weight gain, lethargy, and seizures.
The move, part of a broader effort to improve early diagnosis, targets a condition that can cause severe developmental delays and organ damage if untreated.
Early detection through newborn screening is expected to significantly improve outcomes.
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El NHS examinará a todos los recién nacidos para detectar un trastorno genético mortal para permitir un tratamiento precoz y mejores resultados.