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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Where can I get answers to my questions about newborn screening?
Get answers to commonly asked questions about the Connecticut Newborn Screening Program (CT NBS).
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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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What are fatty acid oxidation disorders?
Learn more about fatty acid oxidation disorders and how they can affect your baby. Learn how the Connecticut Newborn Screening Program can detect these disorders early os they can be treated.
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Where can I find a full list of newborn disorders?
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 information and resources are there for healthcare providers about the Newborn Screening Program?
Get information for providers about the Connecticut Newborn Screening Program. Find procedures around how babies are screened for metabolic and genetic disorders at birth.
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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.
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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 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 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 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 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 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 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 unclassified disorders are screened for?
Learn more about other disorders and how they can affect your baby. Learn how the Connecticut Newborn Screening Program can detect these disorders early os they can be treated.
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What is Biotinidase Deficiency?
Learn more about biotidinase deficiency. Find out about newborn screening for biotidinase deficiency, signs and symptoms, what happens next, and more.
Newborn screening