Newborn screening for cystic fibrosis

Clinical Reviews in Allergy and Immunology

Volumn 35, Issue 3, 2008, Pages 107-115

  Sharp, Jack K ^a   Rock, Michael J ^b  

^a UNIVERSITY AT BUFFALO   (United States)

^b University of Wisconsin Health   (United States)

Author keywords

Cystic fibrosis; Cystic fibrosis transmembrane regulator (CFTR) mutation; Immunoreactive trypsinogen (IRT); Newborn screening; Nutrition; Pseudomonas aeruginosa; Pulmonary disease

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR; TRYPSINOGEN;

ALGORITHM; CLINICAL TRIAL; CONCEPTION; CYSTIC FIBROSIS; DISEASE ASSOCIATION; DISEASE COURSE; DNA SEQUENCE; ENZYME BLOOD LEVEL; ENZYME REPLACEMENT; FORCED EXPIRATORY VOLUME; GENE MUTATION; GENETIC RISK; HETEROZYGOTE; HUMAN; LUNG FUNCTION; MALNUTRITION; NEWBORN; NEWBORN SCREENING; NUTRITIONAL ASSESSMENT; OBSERVATIONAL STUDY; PANCREAS INSUFFICIENCY; REVIEW; SWEAT TEST; SYMPTOM; UNITED STATES; ZINC DEFICIENCY; CAUCASIAN; CHEMISTRY; GENETICS; MANDATORY TESTING; METHODOLOGY; NUCLEOTIDE SEQUENCE; NUTRITIONAL DISORDER; PATHOPHYSIOLOGY; PSEUDOMONAS INFECTION; RESPIRATORY TRACT INFECTION; SWEAT;

ALGORITHMS; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DNA MUTATIONAL ANALYSIS; EUROPEAN CONTINENTAL ANCESTRY GROUP; HUMANS; INFANT NUTRITION DISORDERS; INFANT, NEWBORN; MANDATORY TESTING; NEONATAL SCREENING; PSEUDOMONAS INFECTIONS; RESPIRATORY TRACT INFECTIONS; SWEAT; UNITED STATES; WISCONSIN;

EID: 59449110426     PISSN: 10800549     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12016-008-8082-1     Document Type: Review

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