Benchellal Z A, Huten N, Danquechin Dorval E, Podeur L, Rahili A, Lemeret S, De Muret A
Service de Chirurgie Générale et Digestive, Hôpital Trousseau, CHU, Tours.
Gastroenterol Clin Biol. 1998 Mar;22(3):343-5.
Ehlers-Danlos syndrome denotes a group of inherited connective tissue diseases comprising nine types. Type IV Ehlers-Danlos syndrome is the most life-threatening form. It is characterized by a type III collagen deficiency resulting in arterial fragility and death from vascular rupture or bowel perforation. This disease involves a col 3A1 gene mutation. We report the case of a 44 year-old woman with type IV Ehlers-Danlos syndrome. The medical history of our patient included bowel necrosis and two vascular ruptures. We indicate data required to establish Ehlers-Danlos syndrome diagnosis and guidelines for patient management.
埃勒斯-当洛综合征是指一组遗传性结缔组织疾病,包括九种类型。IV型埃勒斯-当洛综合征是最危及生命的类型。其特征是III型胶原蛋白缺乏,导致动脉脆弱,可因血管破裂或肠穿孔而死亡。这种疾病涉及col 3A1基因突变。我们报告一例44岁IV型埃勒斯-当洛综合征女性患者。我们患者的病史包括肠坏死和两次血管破裂。我们指出了确诊埃勒斯-当洛综合征所需的数据以及患者管理指南。