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NEWBORN SCREENING SERVICESINTRODUCTION Newborn screening is performed as mandated by Georgia Law. Effective January 1, 2007, Georgia law (OLGA 31126 & 31127) and Rules and Regulations (Chapter 290524)
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How to fill out newborn screening services

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Step 1: Obtain the necessary forms for newborn screening services.
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Step 2: Fill out the personal information section of the forms, including the baby's name, date of birth, and contact information.
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Step 3: Provide information about the baby's parents, including their names, addresses, and contact numbers.
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Step 4: Fill out the medical history section, providing details about any known medical conditions or family history of diseases.
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Step 5: Follow the instructions for collecting the baby's blood sample. This may involve pricking the baby's heel and placing a few drops of blood on the designated area of the form or a special filter paper.
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Step 6: Complete any additional sections required by the specific newborn screening program, such as additional tests or consent forms.
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Step 7: Review the completed forms for accuracy and make any necessary corrections.
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Step 8: Submit the forms and the baby's blood sample to the designated newborn screening laboratory as per the instructions provided.
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Step 9: Await the results of the newborn screening tests, which will typically be communicated to you by mail or phone.
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Step 10: Follow any recommended follow-up or additional testing based on the results of the newborn screening.

Who needs newborn screening services?

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Newborn screening services are necessary for all newborn babies.
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Babies are typically screened within the first few days of their life to identify any potential health conditions that may require early intervention.
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The screening helps to detect disorders that may not be apparent at birth but can lead to significant health issues if left untreated.
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Parents, healthcare providers, and governments consider newborn screening services essential to ensure the timely diagnosis and management of various genetic, metabolic, and congenital disorders in infants.
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Even if a baby appears healthy, they should still undergo newborn screening as some conditions may not exhibit symptoms until later in infancy.
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Screening allows for early detection and treatment, which can greatly improve the outcomes and quality of life for affected infants.
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Newborn screening services are a public health program that involves testing newborn babies for certain disorders.
Healthcare providers or facilities responsible for the care of newborn babies are required to file newborn screening services.
Newborn screening services are usually filled out by healthcare providers using specific forms or online platforms provided by the relevant health authority.
The purpose of newborn screening services is to detect and treat certain disorders in newborn babies early on, before symptoms appear, to prevent serious health issues.
Newborn screening services typically require information such as the baby's name, birthdate, test results, and any family history of relevant disorders.
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