"Sack–Barabas syndrome"

-ecchymotic EDS * EDS IV * Ehlers-Danlos syndrome type 4 * Sack-Barabas syndrome * Vascular EDS * vEDS * Prevalence: Unknown * Inheritance: Autosomal recessive or Autosomal dominant * Age of onset: Infancy, Neonatal * * ICD-10: Q79.6 * OMIM: 130050 * UMLS: C0268338 * MeSH: - * GARD: 2082 * MedDRA: -SummaryEpidemiologyThe true prevalence of vascular Ehlers-Danlos syndrome (vEDS

* Spondyloepimetaphyseal dysplasia, Strudwick type * Kniest dysplasia (see also C2/11) COL3: * Ehlers–Danlos syndrome, types 3 & 4 * Sack–Barabas syndrome

* Spondyloepimetaphyseal dysplasia, Strudwick type * Kniest dysplasia (see also C2/11) COL3: * Ehlers–Danlos syndrome, types 3 & 4 * Sack–Barabas syndrome