Ehlers-Danlos Syndrome
Arthrochalasia Ehlers-Danlos Syndrome
aEDS
Arthrochalasia EDS is distinguished by severe generalized joint hypermobility and congenital hip dislocation. It is autosomal dominant and rare, with collagen processing defects underlying connective tissue fragility. Early orthopedic and developmental support is often important.
- Prevalence
- Very rare
- Inheritance
- Autosomal dominant
- Screened at Birth
- No
- On RUSP
- No
About This Data
This disorder is part of the Cureledger rare disease data corpus. We are building privacy-preserving natural history datasets and advocacy tools for rare disease communities. Data is maintained by clinical advisors and the patient community.