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Inquilinus limosus isolated from a cystic fibrosis patient: first UK report

R P D Cooke1, W A O'Neill, J Xu

  • 1Department of Medical Microbiology, District General Hospital, Eastbourne, East Sussex. richard.cooke@aintree.nhs.uk

British Journal of Biomedical Science
|October 4, 2007
PubMed
Abstract

No abstract available in PubMed .

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Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
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