What disease can be hidden behind a diagnosis of atypical cystic fibrosis?
Authors:
L. Marušiaková 1; P. Ďurdík 1; I. Bacmaňáková 1; Z. Sňahničanová 1; L. Šofranková 1; O. Petrovičová 1; M. Kuchta 2; J. Buchanec 1
Authors‘ workplace:
Klinika detí a dorastu, Univerzita Komenského v Bratislave, Jesseniova lekárska fakulta v Martine, Martin
prednosta prof. MUDr. P. Bánovčin, CSc.
1; Klinika detí a dorastu, Univerzita Pavla Jozefa Šafárika v Košiciach, Lekárska fakulta, Košice
prednostka doc. MUDr. I. Schusterová, PhD.
2
Published in:
Čes-slov Pediat 2016; 71 (2): 80-86.
Category:
Case Report
Overview
What disease can be hidden behind a diagnosis of atypical cystic fibrosis?
In our case report we present 11-year-old girl treated by pulmonologist for atypical cystic fibrosis with pulmonary manifestations. Since birth she has been suffering from recurrent respiratory infections, chronic wet cough and persistent accumulation of thick mucus. She has a mild obstructive ventilatory defect and bronchiectasis in the right middle lobe of the lung.
In this case report we want to point out the similarity of clinical signs of congenital diseases affecting mucociliary clearance and the importance and possibilities of differential diagnosis.
Key words:
mucociliary clearance, atypical cystic fibrosis, primary ciliary dyskinesia, high-speed video microscopy
Sources
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Neonatology Paediatrics General practitioner for children and adolescentsArticle was published in
Czech-Slovak Pediatrics
2016 Issue 2
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