Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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ciliary dyskinesia

4 articoli — 2003-2020

RI Casi indimenticabili
Polmoniti ricorrenti

G. Riccio

2020/10 — pag. 659-660 — DOI

The paper describes the case of an adolescent with recurrent pneumonia with lobar bronchiectasis. The Authors suggest that a chest CT should always be performed after a second episode of typical localized pneumonia but even after a fourth, less de...

EL Caso contributivo
Cos'è la sindrome di Jeune e quando pensarciDescrizione di un caso clinico

B. Vergara, C. Muratori, L. Mambelli, A. Zucchini, R. Iannace, G. Parmeggiani, A. Sensi, F. Marchetti

2018/2

Jeune syndrome, also known as asphyxiating thoracic dystrophy, is a rare autosomal recessive skeletal dysplasia characterised by narrow chest, short skull and skeletal abnormalities, which include, among other things, a “trident” appearance of the ac...

RI Pagine elettroniche ; Caso Contributivo
Diagnosi neonatale di discinesia ciliare

E. Palumbo, G. Nasca, C. Malorgio, M. Branchi, G. Pellegrini

2008/2 — pag. 123-124

Primary ciliary dyskinesia is a rare, autosomal recessive genetic disease resulting from an abnormal ultra structural morphology of cilia. Such disease is rarely recognized in neonatal period. Recently, unexplained neonatal respiratory distress has b...

RI Problemi non correnti
Il bambino con tosse cronica e bronchiectasie: inquadramento e proposte terapeutiche

C. Braggion, U. Pradal, A. Delmarco, M. Carli

2003/6 — pag. 371-380

Little is known about the prevalence of bronchiectasis (BR) in paediatric age. However, outside the case of cystic fibrosis (CF), they seem to be rare. The BR can be localised or disseminated. For the former, the most common etiology is post-infect...