Ehlers-Danlos Syndrome
Kyphoscoliotic Ehlers-Danlos Syndrome
kEDS
Kyphoscoliotic EDS combines congenital or early-onset kyphoscoliosis with generalized joint laxity and often diminished muscle tone. It follows an autosomal recessive inheritance pattern and is very rare compared with hypermobile EDS. Orthopedic, rehabilitation, and genetic evaluation guide long-term care.
- Prevalence
- Very 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.