Kids in America: Newborn Screening for Cystic Fibrosis

Within the last year, all 50 states in the United States have adopted newborn screening (NBS) protocols for cystic fibrosis (CF), the most common fatal autosomal recessive disease among Caucasian populations. In this overview, we discuss the rationale for implementing NBS for CF and discuss the diff...

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Vydané v:Laboratory medicine Ročník 42; číslo 10; s. 595 - 601
Hlavní autori: Bender, Laura M., Cotten, Steven W., Willis, Monte S.
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Chicago Oxford University Press 01.10.2011
Predmet:
Adoption
Algorithms
Cystic fibrosis
Deoxyribonucleic acid
DNA
Genes
Genetic counseling
Medical genetics
Medical research
Medical screening
Mortality
Mutation
Newborn babies
Newborn infants
Proteins
Rodents
Studies
ISSN:0007-5027, 1943-7730
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Abstract Within the last year, all 50 states in the United States have adopted newborn screening (NBS) protocols for cystic fibrosis (CF), the most common fatal autosomal recessive disease among Caucasian populations. In this overview, we discuss the rationale for implementing NBS for CF and discuss the different testing algorithms states have adopted. Based on studies in the United States, Australia, and the United Kingdom, these measures will likely lead to less severe disease, prolonged life, and more cost-effective management of CF in the long run. Keywords: cystic fibrosis, newborn screen, trypsinogen, IRT
AbstractList Within the last year, all 50 states in the United States have adopted newborn screening (NBS) protocols for cystic fibrosis (CF), the most common fatal autosomal recessive disease among Caucasian populations. In this overview, we discuss the rationale for implementing NBS for CF and discuss the different testing algorithms states have adopted. Based on studies in the United States, Australia, and the United Kingdom, these measures will likely lead to less severe disease, prolonged life, and more cost-effective management of CF in the long run.
Within the last year, all 50 states in the United States have adopted newborn screening (NBS) protocols for cystic fibrosis (CF), the most common fatal autosomal recessive disease among Caucasian populations. In this overview, we discuss the rationale for implementing NBS for CF and discuss the different testing algorithms states have adopted. Based on studies in the United States, Australia, and the United Kingdom, these measures will likely lead to less severe disease, prolonged life, and more cost-effective management of CF in the long run. Keywords: cystic fibrosis, newborn screen, trypsinogen, IRT
Within the last year, all 50 states in the United States have adopted newborn screening (NBS) protocols for cystic fibrosis (CF), the most common fatal autosomal recessive disease among Caucasian populations. In this overview, we discuss the rationale for implementing NBS for CF and discuss the different testing algorithms states have adopted. Based on studies in the United States, Australia, and the United Kingdom, these measures will likely lead to less severe disease, prolonged life, and more cost-effective management of CF in the long run. [PUBLICATION ABSTRACT]
Audience Academic
Author Cotten, Steven W.
Willis, Monte S.
Bender, Laura M.
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CitedBy_id crossref_primary_10_1002_ppul_26209
crossref_primary_10_1016_j_chroma_2014_06_091
crossref_primary_10_1016_j_nurpra_2019_01_020
crossref_primary_10_1016_j_cppeds_2013_05_001
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Snippet Within the last year, all 50 states in the United States have adopted newborn screening (NBS) protocols for cystic fibrosis (CF), the most common fatal...
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SubjectTerms Adoption
Algorithms
Cystic fibrosis
Deoxyribonucleic acid
DNA
Genes
Genetic counseling
Medical genetics
Medical research
Medical screening
Mortality
Mutation
Newborn babies
Newborn infants
Proteins
Rodents
Studies
Title Kids in America: Newborn Screening for Cystic Fibrosis
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