Hunter G C, Malone J M, Moore W S, Misiorowski R L, Chvapil M
Arch Surg. 1982 Apr;117(4):495-8. doi: 10.1001/archsurg.1982.01380280075015.
Ehlers-Danlos syndrome (EDS) is clinically and genetically a heterogenous disorder of connective tissue synthesis. Seven clinical types of this disease have been identified and the underlying biochemical defects defined in types IV through VII. Unfortunately, most patients with major vascular complications of EDS have few, if any of the commonly recognized musculoskeletal and cutaneous abnormalities. Recognition of the correct diagnosis and the application of accepted vascular surgical techniques may improve the morbidity and mortality for these patients.
埃勒斯-当洛综合征(EDS)在临床和遗传学上是一种结缔组织合成的异质性疾病。已确定该疾病有七种临床类型,并明确了IV型至VII型的潜在生化缺陷。不幸的是,大多数患有EDS主要血管并发症的患者几乎没有(如果有的话)常见的肌肉骨骼和皮肤异常。正确诊断并应用公认的血管外科技术可能会改善这些患者的发病率和死亡率。