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Ultima descărcare din IBN: 2024-03-03 18:23 |
Căutarea după subiecte similare conform CZU |
616.24-003.4-056.7-036(478) (1) |
Patologia sistemului respirator. Tulburări ale organelor de respiraţie (760) |
SM ISO690:2012 MUNTEANU, Oxana. Fibroza chistică la adult: realizări și perspective in Republica Moldova. In: Buletin de Perinatologie, 2020, nr. 4(89), pp. 33-38. ISSN 1810-5289. |
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Buletin de Perinatologie | ||||||
Numărul 4(89) / 2020 / ISSN 1810-5289 | ||||||
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CZU: 616.24-003.4-056.7-036(478) | ||||||
Pag. 33-38 | ||||||
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Rezumat | ||||||
Cystic fibrosis isan autosomal recessive disorder, due to mutations in the cystic fi brosis transmembrane conductance regulator (CFTR) gene, with the highest prevalence in Europe. The purpose of this review is to highlight the comorbidities caused by epithelial cell dysfunction occur in the adults with cystic fi brosis and the new therapies that have been developed to restore CFTR function. Once considered a pediatric disease with a poor prognosis, nowadays the patients with cystic fibrosis can expect to live well into adulthood. The increasing number of adult patients with cystic fi brosis and co-morbidities requires a multidisciplinary approach to optimize the management of these patients. |
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Cuvinte-cheie cystic fibrosis, adult, CFTR modulators, bronchiectasis, comorbidities, муковисцидоз, взрослые, модуляторы МВТР, бронхоэктазы, сопутствующие заболевания |
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