Cystic Fibrosis (CF) Mutations Course
Gain expertise in cystic fibrosis mutations confidently. The course assists clinicians in understanding CFTR genetics, devising testing approaches, interpreting variants, and providing family counselling to offer precise diagnoses, effective reports, and improved care for children suffering from cystic fibrosis.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This Cystic Fibrosis Mutations Course equips you with essential skills to analyse CFTR gene variants, choose appropriate testing methods, and combine sweat chloride tests with genetic findings for accurate diagnosis. You will master ACMG/AMP and ClinGen guidelines, utilise important CFTR databases, evaluate family risks, explore reproductive choices, and prepare precise reports and counselling documents for challenging paediatric cases.
Elevify advantages
Develop skills
- Prepare clear and brief genetic reports for CF, covering methods, results, and recommendations.
- Analyse CFTR variants using ACMG/ClinGen guidelines and evidence from databases.
- Develop diagnostic pathways for CF integrating sweat tests, genetic profiles, and clinical features.
- Select best CFTR tests including panels, NGS, CNV detection, and functional studies.
- Advise CF families on risks, uncertain variants, and family planning options.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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