Article
Genotype-phenotype association in infants with cystic fibrosis at the time of diagnosis.
Pediatric research - 1 Dec 1998
Kraemer R, Birrer P, Liechti-Gallati S
Abstract excerpt
The relationship between the most common disease-causing mutations, the clinical manifestation, and lung function was prospectively assessed in 60 infants (33 females, 27 males) with cystic fibrosis at time of diagnosis (age: 7.2 months; range: 0.8-23.8 months). Lung function was assessed by infa...
Topics
- Bacteria
- Cystic Fibrosis
- Cystic Fibrosis Transmembrane Conductance Regulator
- Female
- Genotype
- Humans
- Infant
- Male
- Mutation
- Phenotype
- Respiratory Function Tests
- Respiratory Mechanics
- Weight Gain