Dermatosparaxis Ehlers-Danlos syndrome
What is Dermatosparaxis Ehlers-Danlos syndrome?
A form of Ehlers-Danlos syndrome (EDS) characterized by extreme skin fragility and laxity, a prominent facial gestalt, excessive bruising and, sometimes, major complications due to visceral and vascular fragility.
Other condition names
- Ehlers-Danlos syndrome type 7C
- Human dermatosparaxis EDS VIIC
- dEDS
Inheritance type
Autosomal recessive
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Infancy
- Neonatal
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