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Assessment Of Neonatal Screening Approaches For Sickle Cell Disease And The Effect Of Early Intervention In Management Of The Disease In Tribal PopulationsCase Record FormFollow up visitInstructions:
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How to fill out neonatal screening and form

01
Obtain the neonatal screening and form from the hospital or healthcare provider.
02
Fill in the personal information of the newborn such as name, date of birth, and gender.
03
Provide family medical history information if applicable.
04
Collect the necessary blood or urine sample as directed by the healthcare provider.
05
Complete any additional requested information on the form.
06
Submit the completed neonatal screening and form to the healthcare provider for processing.

Who needs neonatal screening and form?

01
Newborn babies who are at risk of certain genetic or metabolic disorders.
02
Parents or guardians of newborn babies who want to ensure early detection and intervention for potential health issues.

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Neonatal screening is a public health program whereby newborns are tested for certain genetic, metabolic, hormonal, and functional conditions. The associated form is a document used to collect and report the results of these screenings.
Typically, hospitals and birthing facilities are required to file neonatal screening and the accompanying form for every newborn before they are discharged.
The neonatal screening form should be filled out by healthcare providers, including details such as the baby's identifying information, screening results, and any necessary follow-up actions based on those results.
The purpose of neonatal screening is to identify newborns at risk for certain conditions early, so that prompt treatment can be initiated, preventing serious health issues or death.
Information that must be reported includes the newborn's name, date of birth, birth weight, screening results, and any abnormal findings that require further testing.
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