Learn more about cystic fibrosis

被引：0

作者：

Mazet, Sandra ^{[1
]}

Desmouliere, Alexis ^{[1
]}

机构：

[1] Fac Pharm, 2 Rue Docteur Marcland, F-87025 Limoges, France

来源：

ACTUALITES PHARMACEUTIQUES | 2024年 / 63卷 / 638期

关键词：

CFTR gene and protein; chloride channel; cystic fibrosis; genetic mutation;

D O I：

10.1016/j.actpha.2024.06.005

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Learn more about cystic fibrosis . Cystic fibrosis is a widespread disease worldwide, and the most common rare hereditary genetic disorder in Western populations. Many organs are affected in cystic fibrosis patients. Lesions are linked to dysfunction of an ion channel, the CFTR protein, whose synthesis can be altered by various types of mutation. Pharmacists must be able to inform patients and their families about this disease. (c) 2024 Elsevier Masson SAS. All reserved

引用

页码：17 / 21

页数：5

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[41] Nontuberculous Mycobacteria in Cystic Fibrosis and Non-Cystic Fibrosis Bronchiectasis [J].

Park, In Kwon ;

Olivier, Kenneth N. .

SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2015, 36 (02) :217-224

[42] Ageing with cystic fibrosis: Classical and emerging comorbidities in adults with cystic fibrosis [J].

Regard, L. ;

Lafoeste, H. ;

Martin, C. ;

Chassagnon, G. ;

Burgel, P. -R. .

REVUE DE PNEUMOLOGIE CLINIQUE, 2018, 74 (05) :279-291

[43] Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients [J].

Onay, T ;

Zielenski, J ;

Topaloglu, O ;

Gokgoz, N ;

Kayserili, H ;

Apak, MY ;

Camcioglu, Y ;

Cokugras, H ;

Akcakaya, N ;

Tsui, LC ;

Kirdar, B .

HUMAN BIOLOGY, 2001, 73 (02) :191-203

[44] Using Cystic Fibrosis Therapies for Non-Cystic Fibrosis Bronchiectasis [J].

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[45] Cystic fibrosis and AA amyloidosis: a survey in the French cystic fibrosis network [J].

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[46] When is cystic fibrosis not cystic fibrosis? The importance of appropriately classifying patients [J].

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[47] First report of cystic fibrosis mutations in Libyan cystic fibrosis patients [J].

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[49] Cystic fibrosis: Achromobacter xylosoxidans colonized patients have more severe respiratory disease [J].

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[50] Multiplex PCR reveals that viruses are more frequent than bacteria in children with cystic fibrosis [J].

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Espasa-Soley, Mateu ;

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