A webinar series dedicated to shining a light on alpha-mannosidosis, an ultra-rare genetic disorder caused by a deficiency of the lysosomal enzyme alpha-mannosidase. The symptoms, severity, and progression of alpha-mannosidosis vary widely between individuals, making diagnosis challenging and often delayed. Minimizing the time to diagnosis is important in ensuring that individuals with alpha-mannosidosis and their families receive timely access to support and specialist MDT care.
Join our expert panel as they explore the diverse symptoms of alpha-mannosidosis, challenges and solutions for timely diagnosis, and best practices for long-term management and multidisciplinary care. The webinars will feature case study examples, panel discussions and audience Q&A.
- To identify the symptoms associated with alpha-mannosidosis and understand how to differentiate this condition from other lysosomal storage disorders
- To explore the patient journey through the lens of a real-life case study example and consider how the path to diagnosis could be improved for individuals and their families
- To understand the importance of an early diagnosis, the barriers to diagnosis and how they can be overcome
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This event is organized and funded by Chiesi Ltd.
This information is intended for healthcare professionals only.
There are no continuing medical education (CME) credits for this event.