The training course focuses on identifying the early indicators of alpha-mannosidosis (AM), a highly uncommon genetic condition caused by a deficiency in the alpha-mannosidase enzyme. Due to the wide range of symptoms, varying severity, and individual progression rates, diagnosing alpha-mannosidosis is often complex and subject to delays. Prompt diagnosis is crucial for providing affected individuals and their families with early access to necessary support and specialized multidisciplinary team (MDT) care.
Our expert presenters delve into the varied symptoms associated with alpha-mannosidosis, address the difficulties in achieving a timely diagnosis, and share effective strategies for sustained management and multidisciplinary treatment. The course includes case studies, actionable guidance, and readings for a comprehensive learning experience."