Cystic Fibrosis Foundation Practice Guidelines for the Management of Infants with CFTR-Related Metabolic Syndrome during the First Two Years of Life and Beyond

Through early detection, newborn screening (NBS) for cystic fibrosis (CF) offers the opportunity for early intervention and improved outcomes. NBS programs screen for hypertrypsinogenemia and most also identify mutations in the CF transmembrane conductance regulator (CFTR) gene. Individuals identifi...

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Detalhes bibliográficos
Publicado no:J Pediatr
Main Authors: Borowitz, D, Parad, R, Sharp, JK, Sabadosa, K, Robinson, KA, Rock, M, Farrell, P, Sontag, M, Rosenfeld, M, Davis, S, Marshall, B, Accurso, F
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6326077/
https://ncbi.nlm.nih.gov/pubmed/19914443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpeds.2009.09.003
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