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Coordinating Centre:

Hospital of Padua
Department of Woman and Child Health
via Giustiniani 3, 35128 Padua
Phone number (Phone): +39 049-8218015
Fax number (fax): +39 049-8215430
E-mail: info@pcd-italia.it

RSS

26|11|13
"Clinical and molecular aspects of primary ciliary dyskinesia (PCD)"

Jerusalem - 29-30 January, 2014 read more

27|09|13
"Up to date on primary ciliary dyskinesia in children"

Pifferi M, Di Cicco M, Piras M, Cangiotti AM, Saggese G. Early Hum Dev. 2013 Aug 21. pii:..read more

4|02|13
"A 20-year experience of electron microscopy in the diagnosis of primary ciliary dyskinesia."

Papon JF, Coste A, Roudot-Thoraval F, Boucherat M, Roger G, Tamalet A, Vojtek AM, Amselem S,..read more

4|02|13
"Twenty-year review of quantitative transmission electron microscopy for the diagnosis of primary ciliary dyskinesia."

Shoemark A, Dixon M, Corrin B, Dewar A.- J Clin Pathol. 2012 Mar;65(3):267-71 read more

News

4|02|13
"A 20-year experience of electron microscopy in the diagnosis of primary ciliary dyskinesia."

 

Papon JF, Coste A, Roudot-Thoraval F, Boucherat M, Roger G, Tamalet A, Vojtek AM, Amselem S, Escudier E. - Eur Respir J. 2010 May;35(5):1057-63. 

 

AbstractTransmission electron microscopy (TEM) analysis of ciliary ultrastructure is classically used for the diagnosis of primary ciliary dyskinesia (PCD). We report our extensive experience of TEM analysis in a large series of patients in order to evaluate its feasibility and results. TEM analysis performed in 1,149 patients with suspected PCD was retrospectively reviewed. Biopsies (1,450) were obtained from nasal (44%) or bronchial (56%) mucosa in children (66.5%) and adults (33.5%). TEM analysis was feasible in 71.4% of patients and showed a main defect suggestive of PCD in 29.9%. TEM was more feasible in adults than in children, regardless of the biopsy site. Main defects suggestive of PCD were found in 76.9% of patients with sinopulmonary symptoms and in only 0.4% of patients with isolated upper and 0.4% with isolated lower respiratory tract infections. The defect pattern was similar in children and adults, involving dynein arms (81.2%) or central complex (CC) (18.8%). Situs inversus was never observed in PCD patients with CC defect. Kartagener syndrome with normal ciliary ultrastructure was not an exceptional condition (10.2% of PCD). In conclusion, TEM analysis is feasible in most patients and is particularly useful for PCD diagnosis in cases of sinopulmonary syndrome of unknown origin.