نتایج جستجو برای: primary ciliary dyskinesia

تعداد نتایج: 653356  

رضایی , محمدصادق, صالح محمدزاده , ایرج, صفار , محمدجعفر, غفاری , جواد,

Primary ciliary dyskinesia and Kartagener's syndrome are rare genetic disorders. There is a ciliary dysfunction in these disorders that cause recurrent infections in respiratory and sinus tracts associated with dextrocardia, chronic vasomotor rhinitis and dextrocardia. The aim of this paper is to report two rare cases of Primary ciliary dyskinesia, including one case of primary ciliary dyskin...

ژورنال: فیض 2019

Background: Asthenozoospermia, as the most prevalent cause of male infertility, is defined as low percentage of progressively motile spermatozoa per ejaculate. It occurs in both non-syndromic and syndromic forms and later it manifests as a part of primary ciliary dyskinesia. In the last decade, with the advent of Next-generation sequencing technologies numerous genes have been introduced in the...

Journal: :international journal of pediatrics 0
seyed javad sayedi department of pediatric pulmonology, neonatal research center, dr sheikh hospital, faculty of medicine, mashhad university of medical sciences, mashhad, iran payam mohammadinejad research center for immunodeficiencies, pediatrics center of excellence, children’s medical center, tehran university of medical sciences, tehran, iran mohammadreza modaresi department of pediatric pulmonary and sleep medicine, children medical center, teharn university of medical sciences, tehran, iran gholamreza azizi department of laboratory medicine, imam hassan mojtaba hospital, alborz university of medical sciences, karaj, iran seyed alireza mahdaviani pediatric respiratory diseases research center, national research institute of tuberculosis and lung diseases (nritld), shahid beheshti university of medical sciences, tehran, iran. asghar aghamohammadi research center for immunodeficiencies, pediatrics center of excellence, children’s medical center, tehran university of medical sciences, tehran, iran.

backgroundbronchiectasis is defined by permanent and abnormal widening of the bronchi. although this process occurs in the context of chronic airway infection and inflammation, since there is no accurate estimation of the etiology of the disease. this study aimed to determine the most important cause of bronchiectasis in tehran, iran.materials and methodsin this retrospective cohort study we us...

Journal: :Paediatrics and Child Health 2007

2014
Jane S Lucas Andrea Burgess Hannah M Mitchison Eduardo Moya Michael Williamson Claire Hogg

Primary Ciliary Dyskinesia Centre, Southampton Children’s Hospital, Southampton NHS Foundation Trust, Southampton, UK Clinical and Experimental Sciences Academic Unit, University of Southampton Faculty of Medicine, Southampton, UK Molecular Medicine Unit and Birth Defects Research Centre, University College London (UCL) Institute of Child Health, London, UK Division of Services for Women and Ch...

Journal: :The European respiratory journal 2004
E Baraldi M F Pasquale A M Cangiotti S Zanconato F Zacchello

Nasal nitric oxide levels are low in patients with primary ciliary dyskinesia, but it is not known whether this defect is already present in the first months of life. The current authors measured nasal nitric oxide in two infants with situs inversus and primary ciliary dyskinesia, diagnosed by electron microscopy at 4 and 6 months of age, and in five healthy control infants. Nasal nitric oxide ...

Journal: :American Journal of Respiratory and Critical Care Medicine 2018

Journal: :The European respiratory journal 2014
Pak-Leung Ho Wai-Ching Sin Jasper Fuk-Woo Chan Vincent Chi-Chung Cheng Kwok-Hung Chan

treatment approaches in children. Eur Respir J 2009; 34: 1264–1276. 3 Bush A, Chodhari R, Collins N, et al. Primary ciliary dyskinesia: current state of the art. Arch Dis Child 2007; 92: 1136–1140. 4 Lucas JS, Walker WT, Kuehni CE, et al. Primary ciliary dyskinesia. In: Cordier J-F, ed. Orphan Lung Diseases. Eur Respir Monogr 2011; 54: 201–217. 5 Jorissen M, Willems T, Van der Schueren B, et al...

Primary Ciliary Dyskinesia (PCD) and Kartagener Syndrome (KS) are rare genetic disorders. PCD occurs in patients with recurrent sino-pulmonary infection, dextrocardia, chronic vasomotor rhinitis, and bronchiectasis. This study reports a rare case of KS for having further awareness of this disease. According to this study, this disease should be considered in patients with recurrent respiratory ...

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