Rare neuromuscular and neurogenetic diseases (diagnosis)

Last Update 5 November 2024
1 already enrolled

About This Course

Rare Neuromuscular and Neurogenetic Diseases: How can we recognise early those that we can treat?

This training course is aimed at healthcare professionals, including general practitioners, paediatricians, neurologists and internists, as well as carers and patients affected by rare neuromuscular and neurogenetic diseases. The aim is to raise awareness and provide training in the early recognition of treatable rare diseases, in order to reduce misdiagnosis and improve patient care.

Learning Objectives

Inborn errors of metabolism in children: when and why to think about them?
Gaucher disease, Mucopolysaccharidosis type I (MPS I)
Acid sphingomyelinase deficiency (ASMD)
Pompe's disease
Fabry disease
Familial amyloidosis
Cardiac amyloidosis
Spinal muscular atrophy
Non-dystrophic myotonia
Autoimmune myasthenia

Material Includes

  • Videos
  • Quizz

Target Audience

  • Caregivers
  • Patients

Curriculum

13 Lessons2h 42m 20s

Introduction

Course presentation00:02:28

Rare diseases & city-hospital links

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Free
Level
All Levels
Duration 2.7 hours
Lectures
13 lectures

Material Includes

  • Videos
  • Quizz
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