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Ehlers-Danlos syndrome(s) A group of inherited (genetic) disorders of connective tissue Named after Edvard Ehlers of Denmark and Henri-Alexandre Danlos of France Villefranche 1997Berlin 1988 Classical TypeGravis (Type I) Mitis (Type II) Hypermobile TypeHypermobile (Type III) Vascular TypeArterial-ecchymotic (Type IV) Kyphoscoliosis Type Ocular-Scoliotic (Type VI) Arthrochalasia Type Arthrochalasia (Type VIIA, B) Dermatosporaxis Type Dermatosporaxis (Type VIIC ) Ehlers-Danlos Syndrome Classifications X-Linked EDS (EDS Type V) Periodontitis type (EDS Type VIII) Familial Hypermobility Syndrome (EDS Type XI) Benign Joint Hypermobility Syndrome Hypermobility Syndrome Progeroid EDS Marfanoid habitus with joint laxity Unspecified Forms Other Variants Brittle cornea syndrome PRDM5 ZNF469 Spondylocheirodysplastic Musculocontractural/adducted thumb clubfoot/Kosho D4ST1 deficient EDS Tenascin-X deficiency Do we add

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