Ucisk oczodołu u 6-letniego chłopca z mukowiscydozą

Mieczysław Chmielik, Anna Gabryszewska, Eliza Brożek

Streszczenie
Cystic fibrosis is one of most common genetically inherited, metabolic diseases connected with mutation of the gene coding a CFTR (cystic fibrosis transmembrane regulator) protein. In the ENT specialist practice it may appear in form of chronic sinusitis, mucocoele, mucopyocoele or polyps. While chronic sinusitis may occur at every age, mucocoele usually appear before the 5^th year of age and polyps after the 4^th year. The treatment is usually multifocal. A case of a boy with cystic fibrosis and mucopyocoele has been described in this paper.

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