Literature DB >> 6448132

The dyskinetic cilia syndrome. Ciliary motility in immotile cilia syndrome.

C M Rossman, J B Forrest, R M Lee, M T Newhouse.   

Abstract

Ciliary motility was studied in three patients with Kartagener syndrome who had previously been found to have absent nasal and pulmonary mucociliary transport and missing dynein arms in nasal cilia. A video system was used to record movement of cilia obtained by nasal brushings for analysis of wave form and beat frequency. Two patterns of abnormal ciliary beat were observed; an oscillating and a rotating type of motion. There was no evidence of planar coordination of metachronicity. This abnormal motion was present in up to 40 percent of cells and the remainder were totally immotile. Thus, in Kartagener syndrome many ciliated cells are motile, but the motion is abnormal. We suggest that "immotile cilia syndrome" is a misnomer, and recommended it be renamed "dyskinetic cilia syndrome."

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Year:  1980        PMID: 6448132     DOI: 10.1378/chest.78.4.580

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  22 in total

1.  Role of macrophage-stimulating protein and its receptor, RON tyrosine kinase, in ciliary motility.

Authors:  O Sakamoto; A Iwama; R Amitani; T Takehara; N Yamaguchi; T Yamamoto; K Masuyama; T Yamanaka; M Ando; T Suda
Journal:  J Clin Invest       Date:  1997-02-15       Impact factor: 14.808

2.  Ultrastructure and movement of the ependymal and tracheal cilia in congenitally hydrocephalic WIC-Hyd rats.

Authors:  A Shimizu; M Koto
Journal:  Childs Nerv Syst       Date:  1992-02       Impact factor: 1.475

Review 3.  Gene mutations in primary ciliary dyskinesia related to otitis media.

Authors:  Manuel Mata; Lara Milian; Miguel Armengot; Carmen Carda
Journal:  Curr Allergy Asthma Rep       Date:  2014-03       Impact factor: 4.806

Review 4.  Defects in the determination of left-right asymmetry.

Authors:  M P Splitt; J Burn; J Goodship
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

5.  The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia.

Authors:  G Pennarun; C Chapelin; E Escudier; A M Bridoux; F Dastot; V Cacheux; M Goossens; S Amselem; B Duriez
Journal:  Hum Genet       Date:  2000-12       Impact factor: 4.132

6.  Measurement of in vitro ciliary beat frequency: a television-video modification of the transmitted light technique.

Authors:  H Teichtahl; P L Wright; R L Kirsner
Journal:  Med Biol Eng Comput       Date:  1986-03       Impact factor: 2.602

7.  Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

Authors:  G Pennarun; E Escudier; C Chapelin; A M Bridoux; V Cacheux; G Roger; A Clément; M Goossens; S Amselem; B Duriez
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

8.  Primary ciliary dyskinesia: evolution of pulmonary function.

Authors:  J Hellinckx; M Demedts; K De Boeck
Journal:  Eur J Pediatr       Date:  1998-05       Impact factor: 3.183

Review 9.  Primary Ciliary Dyskinesia: An Update on New Diagnostic Modalities and Review of the Literature.

Authors:  Rizwana Popatia; Kenan Haver; Alicia Casey
Journal:  Pediatr Allergy Immunol Pulmonol       Date:  2014-06-01       Impact factor: 1.349

10.  Dyskinetic cilia syndrome: clinical, radiographic and scintigraphic findings.

Authors:  S Reyes de la Rocha; T J Pysher; J C Leonard
Journal:  Pediatr Radiol       Date:  1987
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