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Classical Ehlers-Danlos syndrome

ORPHA:287· ICD-10 Q79.6

Definition

A rare inherited connective tissue disorder characterized by skin hyperextensibility, widened atrophic scars, and generalized joint hypermobility.

Prevalence
1-9 / 100 000
Inheritance
Autosomal dominant
Age of onset
Childhood, Infancy, Neonatal