Newborn Genetic Screening
Newborn Genetic Screening
Newborn Genetic Screening included inherited hearing loss and pharmacogenetics to prevent or reduce severe result and identify potential treatment and management.
Who should consider Newborn Genetic Screening?
- All newborn infants
- Babies from parents with family history of inherited hearing loss
- Babies from parents with personal or family history of adverse drug reactions to medications
- Parents who would like to know baby’s hearing and drug related genetic status
Flow Chart of Newborn Genetic Screening
If your clinic or physicians are interested in our services or need more information, please feel free to email us: GGA@GGA.Asia
