| Literature DB >> 15332739 |
K P Dawson1, P M Frossard, B Al-Awar.
Abstract
We compared the clinical severity associated with the two cystic fibrosis (CF) mutations S549R(T-->G) and deltaF508. Clinical and biochemical variables of CF were compared in two age- and sex-matched groups of CF children in the United Arab Emirates (UAE). The clinical severity of mutations S549R(T-->G) and deltaF508 showed comparable patterns, with very low Shwachman scores and high sweat chloride levels. We conclude that patients homozygous for the CF mutations deltaF508 and S549R(T-->G) have a severe clinical presentation and illness and are indistinguishable on clinical grounds.Entities:
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Year: 2001 PMID: 15332739
Source DB: PubMed Journal: East Mediterr Health J ISSN: 1020-3397 Impact factor: 1.628