Related Experiment Video For CFTR-related disorder
Updated: May 31, 2026

Implementation of Non-invasive Point of Care Transient Elastography for Evaluation of Liver Disease in Pediatric Populations with Cystic Fibrosis
Published on: August 29, 2025
The Diagnostic Complexities of Cystic Fibrosis: When to Think of It and What to Do?
Ladina Weitnauer1, Nicholas J Simmonds1,2
1Adult Cystic Fibrosis Centre, Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, SW3 6NP London, UK.
Abstract:
Cystic fibrosis (CF) is one of the most common life-shortening hereditary disorders, caused by a defect in the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This defect causes multi-system disease, but primarily it affects the lungs and pancreas. Over 2000 CFTR gene variants have been identified; these can result in variable CFTR protein function and, consequently, a diverse clinical phenotype. CF is not only diagnosed in children but also in adults and is present in non-White populations. In adults, CF often presents with an atypical phenotype, usually due to residual CFTR protein function, which can be caused by rare CFTR variants. As a result, diagnosing CF in adults can be challenging. In this review, we discuss who should be considered for CF, how and where the diagnosis is made, and why a timely CF diagnosis is important for all patients, as well as their families.
Related Concept Videos
Cystic Fibrosis: Management
Sinus disease and chronic sinusitis...
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Chronic Obstructive Pulmonary Disease-IV: Assessement and Diagnostic Studies
Medical History
Chronic Obstructive Pulmonary Disease-I: Introduction
Chronic Pancreatitis II: Collaborative Care
Assessment:
Pneumonia III: Complications and Assessment

