Even though targeted genetic tests are now available, the diagnosis of Marfan syndrome is still mainly based on specific clinical criteria, in particular the revised Ghent classification. The broad phenotypic continuum ranges from mild manifestations to severe and rapidly progressive neonatal multi-organ disease. Timely diagnosis is of crucial importance in order to provide those affected with adequate treatment measures. A multidisciplinary approach is advocated for this.
Autoren
- Mirjam Peter, M.Sc.
Publikation
- HAUSARZT PRAXIS
Related Topics
You May Also Like
- Practice Management
Improved quality of care aims for satisfied patients
- Chemsex - MSM, sex, chrystal meth & co.
Medical and psychosocial perspectives
- Bladder cancer
Tuberculosis vaccination reduces recurrences
- Oral JAK-i in atopic dermatitis
Benefits and risks: What does the current data say?
- Chronic lung diseases
Sarcopenia and malnutrition in the context of pneumological rehabilitation
- Sleep-wake disorders in pneumology practice
Patience, knowledge and persistence in therapy
- Cardiovascular risk and obesity
Pathomechanisms, secondary prevention and treatment options
- Oxidative stress and neurodegeneration