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NEWBORN GENETIC AND METABOLIC DIAGNOSTIC EVALUATION This prior approval is limited to outpatient examinations and laboratory studies needed to confirm a diagnosis suspected on the basis of an abnormal
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01
Collect a blood sample from the newborn within 24-48 hours of birth.
02
Ensure that the blood sample is collected on a specific filter paper designed for genetic and metabolic testing.
03
Fill out all necessary information on the filter paper including the newborn's name, date of birth, and any relevant medical history.
04
Allow the blood sample to dry completely on the filter paper before sending it to the laboratory for testing.

Who needs newborn genetic and metabolic?

01
Newborns who are at risk of genetic or metabolic disorders based on family history or medical conditions.
02
Newborns who show symptoms of genetic or metabolic disorders such as developmental delays, feeding difficulties, or abnormal physical characteristics.
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Newborn genetic and metabolic refers to the screening processes designed to identify and manage inherited metabolic disorders in infants shortly after birth, ensuring early intervention and treatment.
Healthcare providers, including hospitals and birthing centers, are required to file newborn genetic and metabolic screenings for each newborn infant.
To fill out newborn genetic and metabolic forms, healthcare providers must collect relevant data about the infant's health, including any symptoms, family history, and the results of the metabolic screening tests.
The purpose of newborn genetic and metabolic screening is to detect potentially life-threatening conditions early, allowing for timely treatment and improved health outcomes for the infant.
The information that must be reported includes the infant's name, date of birth, details of the screening results, and any follow-up actions taken based on those results.
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