Rare neuromuscular and neurogenetic diseases
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 presentation00:00:52
Rare diseases & city-hospital links
Your Instructors
Free
Material Includes
- Videos
- Quizz
