Newborn screening
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What is the CT Newborn Screening Program?
Learn more about the Connecticut Newborn Screening Program (CT NBS). Learn how screening can detect metabolic and genetic disorders in babies so they can be treated.
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Sickle Cell Trait
Learn more about sickle cell trait and how it can affect your newborn.
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Newborn and prenatal screening
Find typical prenatal testing and newborn screening performed in Connecticut. Always consult with your healthcare provider for more information.
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Connecticut Newborn Screening Program Education and Fact Sheets
Connecticut Newborn Screening Program Fact Sheets
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What is Hemoglobin C Trait?
Hemoglobin C Trait Information
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What is Congenital Cytomegalovirus?
Learn more about congenital cytomegalovirus. Find out about newborn screening for congenital cytomegalovirus, signs and symptoms, what happens next, and more.
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What information and resources are there for parents about the Newborn Screening Program?
Get information for new parents about the Connecticut Newborn Screening Program. Find out how babies are screened for metabolic and genetic disorders at birth.
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What is on the Connecticut Newborn Screening Panel?
Find a full list of disorders that can be detected as part of the Connecticut Newborn Screening Program (CT NBS).
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What is the Connecticut Newborn Screening Panel?
Find out more information about the Connecticut Newborn Screening Panel, based on the Recommended Uniform Screening Panel (RUSP) from the federal Department of Health and Human Services.
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What is Congenital Hypothyroidism?
Learn more about congenital hypothyroidism. Find out about newborn screening for congenital hypothyroidism, signs and symptoms, what happens next, and more.
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What is Glycogen Storage Disease, Type II (Pompe Disease)?
Learn more about glycogen storage disease, type II (Pompe Disease). Find out about newborn screening for Pompe Disease, signs and symptoms, what happens next, and more.
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What is Mucopolysaccharidosis Type 1?
Learn more about mucopolysaccharidosis type 1. Find out about newborn screening for mucopolysaccharidosis type 1, signs and symptoms, what happens next, and more.
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What is Mucopolysaccharidosis Type 2?
Learn more about mucopolysaccharidosis type 2. Find out about newborn screening for mucopolysaccharidosis type 1, signs and symptoms, what happens next, and more.
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What is Tyrosinemia?
Learn more about tyrosinemia. Find out about newborn screening for tyrosinemia, signs and symptoms, what happens next, and more.
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What is Galactosemia?
Learn more about galactosemia. Find out about newborn screening for galactosemia, signs and symptoms, what happens next, and more.
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What is X-Linked Adrenoleukodystrophy?
Learn more about X-linked adrenoleukodystrophy. Find out about newborn screening for X-linked adrenoleukodystrophy, signs and symptoms, what happens next, and more.
Newborn screening