Literature DB >> 27797861

Diagnosis of cystic fibrosis in a patient of Egyptian background.

Rie Yoshida1, Bobby Ruge1.   

Abstract

Cystic fibrosis (CF) is the most common genetically inherited condition in European-derived populations. However, it is being increasingly recognised in other populations, including people of Asian, Black African and Caribbean descent. We present a case detailing the diagnosis of CF in a 12-year-old patient of Egyptian background who had been treated for difficult asthma. In doing so, we aim to highlight the importance of considering CF in all patients, regardless of ethnicity. 2016 BMJ Publishing Group Ltd.

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Year:  2016        PMID: 27797861      PMCID: PMC5073578          DOI: 10.1136/bcr-2016-217072

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  3 in total

Review 1.  Cystic fibrosis.

Authors:  Jane C Davies; Eric W F W Alton; Andrew Bush
Journal:  BMJ       Date:  2007-12-15

2.  Early diagnosis of cystic fibrosis in Jordanian children.

Authors:  H M Nazer
Journal:  J Trop Pediatr       Date:  1992-06       Impact factor: 1.165

3.  Profile of cystic fibrosis in a single referral center in Egypt.

Authors:  Mona M El-Falaki; Walaa A Shahin; Noussa R El-Basha; Aliaa A Ali; Dina A Mehaney; Mona M El-Attar
Journal:  J Adv Res       Date:  2013-07-15       Impact factor: 10.479

  3 in total
  1 in total

1.  Screening for the Most Common Mutations of CFTR Gene among Egyptian Children with Difficult-to-Treat Asthma.

Authors:  Mohammad Al-Haggar; Engy Osman; Abdel-Rahman Eid; Tarek Barakat; Samar El-Morsi
Journal:  J Pediatr Genet       Date:  2020-02-03
  1 in total

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