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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
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.