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Case-Based Approach on Teenager with Cystic Fibrosis: Chronic Pulmonary and Pancreatic Complications
Article Information
Md. Abdur Rahman
A 16-year-old girl with a history of inability to grow, perpetual breathing difficulties, and symptoms of pancreatic insufficiency presented to the clinic. Though her symptoms had lasted many years, a clear diagnosis was not made until recently. Homologous ΔF508 mutation discovered through genetic testing supported the diagnosis of cystic fibrosis (CF). Particularly in teenagers with mild or concurrent symptoms, this case illustrates the need for early diagnosis of CF. Furthermore, it stresses how important a multidisciplinary approach to therapy is in improving the quality of life and clinical results for CF patients.