Ehlers-Danlos Syndrome

被引：0

作者：

Deren-Wagemann, Izabela ^{[1
]}

Kuliszkiewicz-Janus, Malgorzata ^{[1
]}

Schiller, Joanna ^{[1
]}

机构：

[1] Wroclaw Med Univ, Dept Hematol Blood Neoplasms & Bone Marrow Transp, PL-50367 Wroclaw, Poland

来源：

ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE | 2010年 / 19卷 / 04期

关键词：

Ehlers-Danlos syndrome; classification; symptoms; CAROTID-CAVERNOUS FISTULA; SYNDROME TYPE-VI; VALVE-REPLACEMENT; ARTERY ANEURYSM; PATIENT; IV; COLLAGEN; MUTATION; RUPTURE;

D O I：

暂无

中图分类号：

R-3 [医学研究方法]; R3 [基础医学];

学科分类号：

1001 ;

摘要：

Ehlers-Danlos syndrome (EDS) is a group of genetically determined vascular purpura. The pathological changes mainly involve joints, skin and the vascular wall. The incidence of the EDS is 1 per 20 000-100 000 births. The defects involve the structure of collagen as well as other enzymes associated with it. Today there are the following types of EDS: classical, hypermobility, vascular, kyphoscoliotic, arthrochalasia and dermatosparaxis. The individual types of EDS are accompanied by complications of heart muscle, respiratory system, gastrointestinal tract, eyes, teeth, periodontal tissues and obstetric problems. The current paper presents issues relating to epidemiology, pathogenesis, clinical manifestations and treatment of various forms of Ehlers-Danlos syndrome (Adv Clin Exp Med 2010, 19, 4, 537-542).

引用

页码：537 / 542

页数：6

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