Cystic fibrosis - Comparison between patients in paediatric and adult age

Revista Portuguesa de Pneumologia (English Edition)

Volumn 23, Issue 1, 2017, Pages 17-21

  Santos, V ^a   Cardoso, A V ^a   Lopes, C ^b   Azevedo, P ^b   Gamboa, F ^c   Amorim, A ^a,d  

^a Universidade do Porto   (Portugal)

^b HOSPITAL DE SANTA MARIA   (Portugal)

^c CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA   (Portugal)

^d University of Porto   (Portugal)

Author keywords

Cystic fibrosis; Cystic fibrosis adult; Cystic fibrosis diagnosis; Cystic fibrosis in childhood; Cystic fibrosis late diagnosis

Indexed keywords

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADULT; ARTICLE; BACTERIUM ISOLATION; BODY MASS; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; CYSTIC FIBROSIS; FEMALE; GENDER AND SEX; GENE MUTATION; GENOTYPE; HUMAN; LIFE EXPECTANCY; LUNG FUNCTION; MAJOR CLINICAL STUDY; MALE; METHICILLIN SUSCEPTIBLE STAPHYLOCOCCUS AUREUS; MORTALITY RATE; OBESITY; PANCREAS FUNCTION; PANCREATIC INSUFFICIENCY; POPULATION RESEARCH; PSEUDOMONAS INFECTION; RETROSPECTIVE STUDY; ADOLESCENT; AGE; CLINICAL TRIAL; COMPARATIVE STUDY; MULTICENTER STUDY;

ADOLESCENT; ADULT; AGE FACTORS; CHILD; CYSTIC FIBROSIS; FEMALE; HUMANS; MALE; RETROSPECTIVE STUDIES;

EID: 85010430613     PISSN: None     EISSN: 21735115     Source Type: Journal    
DOI: 10.1016/j.rppnen.2016.07.002     Document Type: Article

References (29)

1. Bush A, Alton EWFW, Davies JC, Griesenbach U, Jaffe A, editors.Cystic fibrosis in the 21st century. Prog Respir Res, vol. 34. Basel:Karger; 2006. p. 2-10.
2. WHO. The molecular genetic epidemiology of cystic fibrosis;2004.
3. Farrell PM. The prevalence of cystic fibrosis in the EuropeanUnion. J Cyst Fibros. 2008;7:450-3.
4. Abreu FA, Dodge JA. Guidelines for the diagnosis and manage-ment of cystic fibrosis. World Health Organization; 1996.
5. Trezise AE, Chambers JA, Wardle CJ, Gould S, Harris A. Expres-sion of the cystic fibrosis gene in human foetal tissues. Hum MolGenet. 1993;2:213-8.
6. Vankeerberghen A, Cuppens H, Cassiman JJ. The cystic fibro-sis transmembrane conductance regulator: an intriguing proteinwith pleiotropic functions. J Cyst Fibros. 2002;1:13-29.
7. Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, et al. Identification of the cystic fibrosis gene:cloning and characterization of complementary DNA. Science.1989;245:1066-73.
8. Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, et al. Identification of the cystic fibrosis gene: chromo-some walking and jumping. Science. 1989;245:1059-65.
9. Ferrari M, Cremonesi L. Genotype-phenotype correlation in cys-tic fibrosis patients. Ann Biol Clin (Paris). 1996;54:235-41.
10. Rowe SM, Miller S, Sorscher EJ. Mechanisms of disease: cysticfibrosis. N Engl J Med. 2005;352:1992-2001.
11. Orenstein BM, Winnie GB, Altman H. Cystic fibrosis: a 2002update. J Pediatr. 2002;140:156-64.
12. De Boeck K, Wilschanski M, Castellani C, Taylor C, Cuppens H, Dodge J, et al. Cystic fibrosis: terminology and diagnosticalgorithms. Thorax. 2006;61:627-35.
13. Cystic Fibrosis Foundation: Patient Registry Annual Data Reportto the Center Directors 2013. Bethesda, Maryland: Cystic Fibro-sis Foundation; 2014.
14. Yankaskas JR, Marshall BC, Sufian B, Simon RH, Rodman D. Cystic fibrosis adult care: consensus conference report. Chest.2004;125 Suppl.:1S-39S.
15. Jerry AN, David MR. Manifestations of cystic fibrosis diagnosedin adulthood. Curr Opin Pulm Med. 2005;11:513-8.
16. Hellerstein HK. Cystic fibrosis of the pancreas in an adult. OhioMed J. 1946;42:616-7.
17. Gardiner KR, Cranley B. Acute presentation of cystic fibrosis inan adult. Postgrad Med J. 1989;65:471-2.
18. Hunt B, Geddes DM. Newly diagnosed cystic fibrosis in middleand later life. Thorax. 1984;40:23-6.
19. Fiel S. Cystic fibrosis in an adult. Emerg Med. 1988;20:109-21.
20. Godby J. Cystic fibrosis in adults. J Miss State Med Assoc.1985;26:161-3.
21. Su CT, Beanblossom B. Typical cystic fibrosis in an elderlywoman. Am J Med. 1989;86:701-3.
22. Gan KH, Veeze HJ, van den Ouweland AM, Halley DJ, Scheffer H, van der Hout A, et al. A cystic fibrosis mutation associatedwith mild lung disease. N Engl J Med. 1995;333:93-9.
23. Gilljam M, Ellis L, Corey M, Zielenski J, Durie P, Tullis DE. Clinicalmanifestations of cystic fibrosis among patients with diagnosisin adulthood. Chest. 2004;126:1215-24.
24. Gan KH, Geus WP, Bakker W, Lamers CB, Heijerman HG. Geneticand clinical features of patients with cystic fibrosis diagnosedafter the age of 16 years. Thorax. 1995;50:1301-4.
25. McWilliams TJ, Wilsher ML, Kolbe J. Cystic fibrosis diagnosed inadult patients. N Z Med J. 2000;113:6-8.
26. Widerman E, Millner L, Sexauer W, Fiel S. Health status andsociodemographic characteristics of adults receiving a cysticfibrosis diagnosis after age 18 years. Chest. 2000;118:427-33.
27. Santis G, Osborne L, Knight RA, Hodson ME. Independent geneticdeterminants of pancreatic and pulmonary status in cystic fibro-sis. Lancet. 1990;336:1081-4.
28. Kristidis P, Bozon D, Corey M, Markiewicz D, Rommens J, Tsui LC,et al. Genetic determination of exocrine pancreatic function incystic fibrosis. Am J Hum Genet. 1992;50:1178-84.
29. Tummler B, Stanke F. Genetic and environmental modifiers ofcystic fibrosis. ERS Monogr. 2014;64:47-64.