Literature DB >> 26362507

Diagnostic Methods in Primary Ciliary Dyskinesia.

Jane S Lucas1, Tamara Paff2, Patricia Goggin3, Eric Haarman4.   

Abstract

Diagnosing primary ciliary dyskinesia is difficult. With no reference standard, a combination of tests is needed; most tests require expensive equipment and specialist scientists. We review the advances in diagnostic testing over the past hundred years, with emphasis on recent advances. We particularly focus on use of high-speed video analysis, transmission electron microscopy, nasal nitric oxide and genetic testing. We discuss the international efforts that are in place to advance the evidence base for diagnostic tests.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Diagnosis; Electron microscopy; Genetics; High speed video analysis; Nitric oxide; Primary ciliary dyskinesia

Mesh:

Year:  2015        PMID: 26362507     DOI: 10.1016/j.prrv.2015.07.017

Source DB:  PubMed          Journal:  Paediatr Respir Rev        ISSN: 1526-0542            Impact factor:   2.726


  11 in total

Review 1.  Prevalence of primary ciliary dyskinesia in consecutive referrals of suspect cases and the transmission electron microscopy detection rate: a systematic review and meta-analysis.

Authors:  Panayiotis Kouis; Panayiotis K Yiallouros; Nicos Middleton; John S Evans; Kyriacos Kyriacou; Stefania I Papatheodorou
Journal:  Pediatr Res       Date:  2016-12-09       Impact factor: 3.756

2.  Early diagnosis effects the prognosis in children with atypical wheeze.

Authors:  Ezgi Ulusoy Severcan; Esen Demir; Figen Gülen; Raziye Burcu Güven Bilgin; Remziye Tanaç
Journal:  Turk Pediatri Ars       Date:  2020-09-23

3.  The effect of a novel LRRC6 mutation on the flagellar ultrastructure in a primary ciliary dyskinesia patient.

Authors:  Yaqian Li; Chuan Jiang; Xueguang Zhang; Mohan Liu; Yongkang Sun; Yihong Yang; Ying Shen
Journal:  J Assist Reprod Genet       Date:  2021-01-05       Impact factor: 3.412

Review 4.  The determination factors of left-right asymmetry disorders- a short review.

Authors:  Andreea Catana; Adina Patricia Apostu
Journal:  Clujul Med       Date:  2017-04-25

5.  The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results.

Authors:  Myrofora Goutaki; Elisabeth Maurer; Florian S Halbeisen; Israel Amirav; Angelo Barbato; Laura Behan; Mieke Boon; Carmen Casaulta; Annick Clement; Suzanne Crowley; Eric Haarman; Claire Hogg; Bulent Karadag; Cordula Koerner-Rettberg; Margaret W Leigh; Michael R Loebinger; Henryk Mazurek; Lucy Morgan; Kim G Nielsen; Heymut Omran; Nicolaus Schwerk; Sergio Scigliano; Claudius Werner; Panayiotis Yiallouros; Zorica Zivkovic; Jane S Lucas; Claudia E Kuehni
Journal:  Eur Respir J       Date:  2017-01-04       Impact factor: 16.671

6.  Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility.

Authors:  Giulia Ascari; Frank Peelman; Pietro Farinelli; Toon Rosseel; Nina Lambrechts; Kirsten A Wunderlich; Matias Wagner; Konstantinos Nikopoulos; Pernille Martens; Irina Balikova; Lara Derycke; Gabriële Holtappels; Olga Krysko; Thalia Van Laethem; Sarah De Jaegere; Brecht Guillemyn; Riet De Rycke; Jan De Bleecker; David Creytens; Jo Van Dorpe; Jan Gerris; Claus Bachert; Christiane Neuhofer; Sophie Walraedt; Almut Bischoff; Lotte B Pedersen; Thomas Klopstock; Carlo Rivolta; Bart P Leroy; Elfride De Baere; Frauke Coppieters
Journal:  Hum Mutat       Date:  2020-02-12       Impact factor: 4.878

7.  Diagnosing primary ciliary dyskinesia: an international patient perspective.

Authors:  Laura Behan; Audrey Dunn Galvin; Bruna Rubbo; Sarah Masefield; Fiona Copeland; Michele Manion; Bernhard Rindlisbacher; Beatrice Redfern; Jane S Lucas
Journal:  Eur Respir J       Date:  2016-08-04       Impact factor: 16.671

8.  Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia.

Authors:  Zuzanna Bukowy-Bieryllo; Maciej Dabrowski; Michał Witt; Ewa Zietkiewicz
Journal:  RNA Biol       Date:  2016-08-12       Impact factor: 4.652

9.  Identification of Pathogenic Mutations and Investigation of the NOTCH Pathway Activation in Kartagener Syndrome.

Authors:  Yongjian Yue; Qijun Huang; Peng Zhu; Pan Zhao; Xinjuan Tan; Shengguo Liu; Shulin Li; Xuemei Han; Linling Cheng; Bo Li; Yingyun Fu
Journal:  Front Genet       Date:  2019-08-22       Impact factor: 4.599

Review 10.  Rare Human Diseases: Model Organisms in Deciphering the Molecular Basis of Primary Ciliary Dyskinesia.

Authors:  Martyna Poprzeczko; Marta Bicka; Hanan Farahat; Rafal Bazan; Anna Osinka; Hanna Fabczak; Ewa Joachimiak; Dorota Wloga
Journal:  Cells       Date:  2019-12-11       Impact factor: 6.600

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