Cystic fibrosis – Comparison between patients in paediatric and adult age

Autor: Carla Lopes, Adelina Amorim, F. Gamboa, V. Santos, A.V. Cardoso, Pilar Azevedo
Rok vydání: 2017
Předmět:
Zdroj: Revista Portuguesa de Pneumologia (English Edition), Vol 23, Iss 1, Pp 17-21 (2017)
ISSN: 2173-5115
DOI: 10.1016/j.rppnen.2016.07.002
Popis: Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians. Although most cases are diagnosed in childhood, diagnosis in adults is apparently increasing. Objective: Evaluate the adult population with CF, comparing patients who were diagnosed before and after 18 years of age. Methods: Retrospective analysis of patients followed in three main medical centres in Portugal in 2012. Comparison of two groups: G1 â patients diagnosed at
Databáze: OpenAIRE