Arthrochalasia Ehlers-Danlos syndrome
What is Arthrochalasia Ehlers-Danlos syndrome?
A form of Ehlers-Danlos syndrome (EDS) characterized by congenital bilateral hip dislocation, severe generalized joint hypermobility with recurrent joint dislocations and subluxations, hyperextensible and/or fragile skin.
Other condition names
- Arthrochalasis multiplex congenita
- EDS VII
- Ehlers-Danlos syndrome type 7
- Ehlers-Danlos syndrome, arthrochalasia type
- aEDS
Inheritance type
Autosomal dominant
Prevalence
- Worldwide: Unknown
Age of Onset
- Infancy
- Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.