Growth in prepubertal children with cystic fibrosis, homozygous for the ΔF508 mutation

Journal of Cystic Fibrosis

Volumn 2, Issue 2, 2003, Pages 76-83

  Keller, Bigna M ^a   Casaulta Aebischer, Carmen ^a   Kraemer, Richard ^a   Schöni, Martin H ^a  

^a UNIVERSITY OF BERN   (Switzerland)

Author keywords

Body mass index; Height; Pulmonary function; Weight

Indexed keywords

ARTICLE; BODY HEIGHT; BODY MASS; BODY WEIGHT; CHILD; CHILD GROWTH; CLINICAL ARTICLE; COHORT ANALYSIS; CORRELATION ANALYSIS; CYSTIC FIBROSIS; DISEASE SEVERITY; FOLLOW UP; FORCED EXPIRATORY VOLUME; GENE MUTATION; GENOTYPE; GROWTH DISORDER; HOMOZYGOSITY; HUMAN; INFANT; LONG TERM CARE; LONGITUDINAL STUDY; LUNG FUNCTION TEST; PEDIATRIC HOSPITAL; PREPUBERTY; PREVALENCE; PROGNOSIS; RESPIRATORY TRACT PARAMETERS; RETROSPECTIVE STUDY; SCORING SYSTEM; STATISTICAL SIGNIFICANCE; SURVIVAL; SWITZERLAND; VITAL CAPACITY;

ADOLESCENT; ANALYSIS OF VARIANCE; BODY HEIGHT; BODY MASS INDEX; BODY WEIGHT; CHILD; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; FORCED EXPIRATORY VOLUME; GENOTYPE; GROWTH DISORDERS; HOMOZYGOTE; HOSPITALS, PEDIATRIC; HUMANS; LINEAR MODELS; LONGITUDINAL STUDIES; MALE; MAXIMAL MIDEXPIRATORY FLOW RATE; MUTATION; PEPTIDE FRAGMENTS; RETROSPECTIVE STUDIES; SWITZERLAND; VITAL CAPACITY;

EID: 0038309278     PISSN: 15691993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1569-1993(03)00023-7     Document Type: Article

References (18)

1. Laursen E.M. Koch C. Petersen J.H. Müller J. Secular changes in anthropometric data in cystic fibrosis patients Acta Paediatr 88 1999 169-174
2. Nir M. Lanng S. Krogh Johansen H. Koch C. Long term survival and nutritional data in patients with cystic fibrosis treated in a Danish centre Thorax 51 1996 1023-1027
3. Collins C.E. MacDonald-Wicks L. Rowe S. O'Loughlin E.V. Henry R.L. Normal growth in cystic fibrosis associated with a specialised centre Arch Dis Child 81 1999 241-246
4. Kraemer R. Rüdeberg A. Hadorn B. Rossi E. Relative underweight in cystic fibrosis and its prognostic value Acta Paediatr 67 1978 33-37
5. Moorcroft A.J. Dodd M.E. Webb A.K. Long-term change in exercise capacity, body mass, and pulmonary function in adults with cystic fibrosis Chest 111 1997 338-343
6. Morison S. Dodge J.A. Cole T.J. Lewis P.A. Coles E.C. Geddes D. Russel G. et-al. Height and weight in cystic fibrosis: a cross sectional study Arch Dis Child 77 1997 497-500
7. Kerem E. Corey M. Kerem B. Rommeus J. Markiewicz D. Levison H. Tsui L.C. Durie P. The relation between genotype and phenotype in cystic fibrosis-analysis of the most common mutation (ΔF508) N Engl J Med 323 1990 1517-1522
8. Al-Jader L. Meredith A. Ryley H. Cheadle J. Maguire S. Owen G. Goodchild M. Harper P. Severity of chest disease in cystic fibrosis patients in relation to their genotypes J Med Genet 29 1992 883-887
9. Johansen H.K. Nir M. Hoiby N. Koch C. Schwartz M. Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutation Lancet 337 1991 631-634
10. Duthie A. Doherty D. Williams C. Scott-Jupp R. Warner J. Tanner M. Williamson R. Mowat A. Genotype analysis for ΔF508, G551D and R553X mutations in children and young adults with cystic fibrosis with and without chronic liver disease Hepatology 15 1992 660-664
11. Borgo G. Gasparini P. Bonizzato A. Cabrini G. Mastella G. Pignatti P.F. Cystic fibrosis: the ΔF508 mutation does not lead to an exceptionally severe phenotype. A cohort study Eur J Pediatr 152 1993 1006-1011
12. Kraemer R. Aebi C. Casaulta Aebischer C. Gallati S. Early detection of lung disease and its association with the nutritional status, genetic background and life events in patients with cystic fibrosis Respiration 67 5 2000 477-490
13. Corey M. Edwards L. Levison H. Knowles M. Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis J Pediatr 131 1997 809-814
14. Kerem E. Kerem B. The relationship between genotype and phenotype in cystic fibrosis Curr Opin Pulm Med 1 1995 450-456
15. Zapletal A. Motoyama E.K. Van De Woestijne K.P. Hunt V.R. Bouhuys A. Maximum expiratory flow-volume curves and airway conductance in children and adolescents J Appl Physiol 26 3 1969 308-316
16. Luther R. Evers H. Seidel R. Durschmied H. Reference values for spirometry exemplified by FVC and FEV1 parameters-Comparison of normal values of the pathophysiology of respiration section and the European Society for Coal and Steel Z Erkr Atmungsorgane 176 1 1991 48-56
17. Prader A. Largo R.H. Molinari L. Issler C. Physical growth of Swiss children from birth to 20 years of age. First Zurich longitudinal study of growth and development Helv Paediatr Acta Suppl 52 1989 1-125
18. Gan K. Veeze H. van den Ouweland A.et-al. A cystic fibrosis mutation associated with mild lung disease N Engl J Med 333 1995 95-99