Literature DB >> 9444381

Ciliary dyskinesia in the nose and paranasal sinuses.

M Jorissen1, B Bertrand, P Eloy.   

Abstract

Primary ciliary dyskinesia is a rare autosomal recessive disorder of which 50% with situs inversus Kartagener's syndrome. Secondary ciliary dyskinesia is a frequent observation, mostly in association with or after respiratory tract infections. Diagnosis and differential diagnosis are mostly based on the typical clinical picture, the absence of mucociliary clearance and ciliary activity and the electron microscopical demonstration of ultrastructural abnormalities. However, these investigations are not always conclusive. Functional and ultrastructural ciliary evaluation after ciliogenesis in tissue culture is essential and crucial.

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Mesh:

Year:  1997        PMID: 9444381

Source DB:  PubMed          Journal:  Acta Otorhinolaryngol Belg        ISSN: 0001-6497


  3 in total

Review 1.  Genetics and pulmonary medicine. 6. Immotile cilia syndrome: past, present, and prospects for the future.

Authors:  B A Afzelius
Journal:  Thorax       Date:  1998-10       Impact factor: 9.139

2.  Ciliary ultrastructure in two sisters with Kartagener's syndrome.

Authors:  Kayoko Tanaka; Akihisa Sutani; Yuka Uchida; Yoshihiko Shimizu; Michio Shimizu; Masumi Akita
Journal:  Med Mol Morphol       Date:  2007-03-29       Impact factor: 2.309

Review 3.  In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases.

Authors:  Zuzanna Bukowy; Ewa Ziętkiewicz; Michał Witt
Journal:  J Appl Genet       Date:  2010-12-02       Impact factor: 3.240

  3 in total

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