COURSE DESCRIPTION
A webinar series dedicated to spotting the early signs of alpha-mannosidosis (AM), 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. Minimising 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 experts 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, practical advice, and audience Q&A.
Language: English
Duration: 30 minutes, followed by 15 minutes of questions from the audience and discussion
Presenter: Presenter: Dr Mercedes Gil-Campos (University of Cordoba, Spain)
LEARNING OBJECTIVES
- The importance of the holistic approach to AM management
- Reviewing the care process and the specialists involved
- Understanding the multidisciplinary team in the MPS and AM patient journey: different speciality perspectives
- Exploring the patient management of alpha-mannosidosis
- Optimising therapeutic outcomes