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visuel parcours 4'
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Rare neuromuscular and neurogenetic diseases (diagnosis)

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Free
Parcours 4

Rare neuromuscular and neurogenetic diseases (diagnosis)

13 Lessons
2.7 hours
All Levels
What you'll learn
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
Get Enrolled
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visuel parcours 4'
Free
All Levels

Rare neuromuscular and neurogenetic diseases (diagnosis)

admin
Free
Parcours 4

Rare neuromuscular and neurogenetic diseases (diagnosis)

13 Lessons
2.7 hours
All Levels
What you'll learn
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
Get Enrolled

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visuel parcours 4'
Free
Parcours 4

Rare neuromuscular and neurogenetic diseases (diagnosis)

13 Lessons
2.7 hours
All Levels

This course is designed for patients being monitored for a …

Free
Get Enrolled
What you'll learn
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

This project is co-financed by the Interreg Alcotra programme

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Tel : 04 92 03 57 57
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27 Bd Pasteur, 06000 Nice

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Repérage précoce des troubles du neurodéveloppement
Maladies neurodégénératives (maladie d’Alzheimer)​
Maladies neuromusculaires et neurogénétiques

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