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Neurogenic arthrogryposis multiplex congenita
Disease definition
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy.
ORPHA:1143
Classification level: DisorderA summary on this disease is available in Deutsch (2017) Español (2017) Français (2017) Italiano (2017) Nederlands (2017)
Detailed information
Guidelines
- Anesthesia guidelines
- Deutsch (2019) - Orphananesthesia
- Czech (2019) - Orphananesthesia
- English (2019) - Orphananesthesia
- Português (2019) - Orphananesthesia
- Español (2019) - Orphananesthesia


Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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