Literature DB >> 10940794

Clinical features associated with a delayed diagnosis of cystic fibrosis.

M McCloskey1, A O Redmond, A Hill, J S Elborn.   

Abstract

BACKGROUND: The majority of patients with cystic fibrosis (CF) are diagnosed in the first decade of life. In a small number of patients, the diagnosis is not made until later.
OBJECTIVE: In this study, the clinical and genetic features of patients diagnosed after the age of 10 were examined.
METHODS: All living patients in Northern Ireland diagnosed prior to 1983, when neonatal screening was introduced, were studied. A total of 103 patients were identified of whom 18 were diagnosed after the age of 10. The relationships between late diagnosis and clinical presentation, sputum microbiology, pancreatic sufficiency, nutritional status, genotype and distance from the regional CF centres was determined by multiple regression analysis.
RESULTS: All 18 late-diagnosed patients had a sweat (chloride >70 mmol/l). Late diagnosis was significantly related to carriage of the R117H mutation (r(2) = 0.45) and pancreatic sufficiency (r(2) = 0.37). There was a weak relationship with pulmonary function (r(2) = 0.09).
CONCLUSIONS: In Northern Ireland, late diagnosis in mainly associated with pancreatic function and carriage of the R117H mutation. Copyright 2000 S. Karger AG, Basel

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Year:  2000        PMID: 10940794     DOI: 10.1159/000029538

Source DB:  PubMed          Journal:  Respiration        ISSN: 0025-7931            Impact factor:   3.580


  8 in total

1.  Diagnosing CF: sweat, blood and years.

Authors:  J S Elborn; J M Bradley
Journal:  Thorax       Date:  2006-07       Impact factor: 9.139

2.  Effects of gender and age at diagnosis on disease progression in long-term survivors of cystic fibrosis.

Authors:  Jerry A Nick; Cathy S Chacon; Sara J Brayshaw; Marion C Jones; Christine M Barboa; Connie G St Clair; Robert L Young; David P Nichols; Jennifer S Janssen; Gwen A Huitt; Michael D Iseman; Charles L Daley; Jennifer L Taylor-Cousar; Frank J Accurso; Milene T Saavedra; Marci K Sontag
Journal:  Am J Respir Crit Care Med       Date:  2010-05-06       Impact factor: 21.405

3.  Delayed cystic fibrosis presentation in children in the absence of newborn screening.

Authors:  A Jackson; L Foley; L Daly; P Fitzpatrick; M Harrington; S Zhou; C Kelleher
Journal:  Ir Med J       Date:  2010-04

4.  Classic respiratory disease but atypical diagnostic testing distinguishes adult presentation of cystic fibrosis.

Authors:  Claire L Keating; Xinhua Liu; Emily A Dimango
Journal:  Chest       Date:  2009-12-04       Impact factor: 9.410

5.  Clinical and laboratory profile of children with Cystic Fibrosis: Experience of a tertiary care center in Pakistan.

Authors:  Danish Abdul Aziz; Abdul Gaffar Billoo; Ahad Qureshi; Misha Khalid; Salman Kirmani
Journal:  Pak J Med Sci       Date:  2017 May-Jun       Impact factor: 1.088

6.  How are the ancient cystic fibrosis patients? Cystic fibrosis diagnosed over 60 years-old.

Authors:  C Prados; M Lerín; J J Cabanillas; L Gómez-Carrera; R Álvarez-Sala
Journal:  Respir Med Case Rep       Date:  2017-03-24

Review 7.  Fertility, Pregnancy and Lactation Considerations for Women with CF in the CFTR Modulator Era.

Authors:  Raksha Jain; Jennifer L Taylor-Cousar
Journal:  J Pers Med       Date:  2021-05-15

8.  CFTR Heterozygotes Are at Increased Risk of Respiratory Infections: A Population-Based Study.

Authors:  Philip M Polgreen; Grant D Brown; Douglas B Hornick; Ferhaan Ahmad; Barry London; David A Stoltz; Alejandro P Comellas
Journal:  Open Forum Infect Dis       Date:  2018-11-01       Impact factor: 3.835

  8 in total

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