Ehlers-Danlos Syndrome
Dermatosparaxis Ehlers-Danlos Syndrome
dEDS
Dermatosparaxis EDS is an extremely rare autosomal recessive disorder with marked skin fragility, bruising, and redundant, soft skin. Wound care and infection prevention are central to management. Genetic confirmation helps family counseling and care planning.
- Prevalence
- Extremely rare
- Inheritance
- Autosomal recessive
- 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.