Neonatology

Newborn Genetic Screening

Newborn genetic screening is the practice of testing every newborn for certain harmful or treatable genetic disorders in newborn infants.  Babies with these conditions appear normal at birth. It is only with time that the conditions affects the baby’s brain or physical development or causes other medical problems. By then the damage may be permanent.  Early diagnosis and treatment can result in normal growth and development and can reduce morbidity and mortality.