Newborn Screening involves the screening of newborns in the first days of their lives for inborn errors of metabolism and certain disorders that can hinder the normal development of the baby. These disorders, are not apparent at the time of the baby's birth, but have potential to cause permanent neurological, cognitive, tactile and physical damage in the child. Early detection of such diseases enable initiating of suitable interventions to prevent concerning conditions in the long run.
The VARIANT nbs system is the established worldwide standard in automated newborn screening for sickle cell disease and other hemoglobin disorders. This sophisticated system detects the presence of hemoglobins S, F, C, D, E and other abnormal hemoglobins. With the VARIANT nbs system, you get the total picture.
The VARIANT nbs system is the established worldwide standard in automated newborn screening for sickle cell disease and other hemoglobin disorders. This sophisticated system detects the presence of hemoglobins S, F, C, D, E and other abnormal hemoglobins. With the VARIANT nbs system, you get the total picture.
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