Abstract
#CysticFibrosis (CF) is a multisystem #geneticdisease whose main
cause of #morbidity and #mortality is progressive impairment of lung
function associated with loss of quality of life and functional
capacity. We report the clinical case of an 18-year-old adolescent
accompanied at
a reference center with #bronchialhyper-secretion, recurrent infections,
bacterial colonization, important obstructive ventilatory disorder, and
pulmonary #computedtomography (CT) showing a heterogeneous pattern. The
authors emphasize the importance of continuous monitoring of
#pulmonary, nutritional and functional parameters, allowing for more
effective early interventions.
Following the Clinical and Functional Status of an #Adolescent with #CysticFibrosis: Case Report by Cássio Daniel Araújo da Silva in BJSTR
