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Nasal potential difference: a clinical diagnostic test for cystic fibrosis.

作者信息

Alton E W, Currie D, Logan-Sinclair R, Warner J O, Hodson M E, Geddes D M

机构信息

Royal Brompton and National Heart Hospital, London, UK.

出版信息

Eur Respir J. 1990 Sep;3(8):922-6.

PMID:2292287
Abstract

Patients with cystic fibrosis (CF) demonstrate a markedly more negative potential difference (PD) across respiratory epithelia than normal or "diseased" controls. A technique is described for the measurement of nasal PD in both children and adults. 145 non-CF subjects showed a mean PD of -19.0 mV (range -2 to -36) in comparison to 60 patients with cystic fibrosis with mean of -46.0 mV (range -32 to -77). Amongst the latter group those with more severe disease had a more negative PD. Measurement of nasal PD is easily learnt and rapidly performed and may provide an additional means of diagnosis for CF.

摘要

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