Learn from the Experts, On Demand

Explore detailed insights into ENT manifestations, the diagnostic pathway, and distinguishing features of AM compared to other lysosomal storage disorders.

Exploring the impact of alpha-mannosidosis on patients and families, with a focus on quality of life, caregiver support, and holistic care.

Understanding alpha-mannosidosis, its clinical features, diagnostic challenges, and the importance of early recognition to improve patient outcomes.

Review of treatment options & multidisciplinary strategies for Alpha-mannosidosis, backed by consensus-based methodologies.

Comprehensive overview of the current and emerging therapies for MPS and the role of multidisciplinary care.

Discussion on the importance of early MPS diagnosis, combining genetics and neuropsychology to improve outcomes.

Discover a detailed case-based discussion on the early detection of MPS, highlighting how variability in presentation can lead to treatment delays.

An in-depth walkthrough of the AM patient journey, from diagnosis to lifelong management, emphasizing the importance of early recognition.

A detailed overview of AM, focusing on the importance of early diagnosis, therapeutic strategies, and multidisciplinary management.

Clinical insights on diagnosing AM, highlighting outlines common clinical signs, phenotype variability and diagnostic challenges.

Discussion on early AM signs, highlighting diagnostic overlap with MPS & other lysosomal disorders.

Review on MLD progression, and emerging treatments, focusing on gene therapy and real-life case studies.

A comprehensive update on newborn screening for MLD, focusing on the importance of early identification and the implications for timely treatment.

Explore the challenges of recognizing early clinical manifestations of MLD and the importance of prompt referral and diagnosis.

Explore the nature of disease and the long-term care and management of individuals diagnosed with AM.

Hearing loss, developmental delay, and behavioral changes are key AM red flags—age-specific algorithms aim to shorten the years-long diagnostic odyssey.

How diagnostic delays, multidisciplinary care, surgical risks, and psychosocial strain shape everyday life for patients with MPS and their families.

Este webinar aborda el diagnóstico y manejo temprano de las mucopolisacaridosis (MPS), proporcionando herramientas clave para mejorar su detección y tratamiento

MPS I spectrum—from Hurler to Scheie—shown through cases of delayed diagnosis, urging pediatricians to spot symptom clusters early and pursue ERT sooner.

Explore how GAG accumulation drives disease, why HSCT and ERT have different strengths, and why newborn screening enables earlier, better outcomes.