The Importance Of Spotting The Early Signs Of Alpha-mannosidosis (AM)

30 minutes
English
Rare Diseases
Alpha-Mannosidosis
AM

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. 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 experts as they explore alpha-mannosidosis's diverse symptoms, challenges, 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.

Learning Objectives

Exploring the early clinical manifestations of MPS and alpha-mannosidosis – What evert HCP should look forExamining the multi-systemic features of the diseases - red flags, signs, symptoms and when to referReviewing the diagnostic approaches to MPS and AM. From suspicion to diagnosis confirmation