Black C M, Gathercole L J, Bailey A J, Beighton P
Br J Dermatol. 1980 Jan;102(1):85-96. doi: 10.1111/j.1365-2133.1980.tb05675.x.
The structure of the collagen fibres of the skin in the Ehlers-Danlos syndrome (ED-S) was studied in eight patients with ED-S Type I, three patients with ED-S Type II and three patients with the X-linked Type V. The results show that the reducible cross-links are present and undergo the same maturation process to non-reducible cross-links as in normal skin. Transmission electron microscopy revealed a normal ultrastructure of the collagen fibrils. At a higher morphological level of organization scanning electron microscopy demonstrated progressive increase in fibre bundle disorder from the X-linked to mitis, to gravis, in which the fibres making up the large fibre bundles demonstrated a considerable inability to aggregate.
对8例Ⅰ型埃勒斯-当洛综合征(ED-S)患者、3例Ⅱ型ED-S患者和3例X连锁Ⅴ型患者的皮肤胶原纤维结构进行了研究。结果表明,可还原交联键存在,并且与正常皮肤一样经历向不可还原交联键的相同成熟过程。透射电子显微镜显示胶原纤维的超微结构正常。在更高的组织形态学水平上,扫描电子显微镜显示从X连锁型到轻型、再到重型,纤维束紊乱逐渐增加,其中构成大纤维束的纤维显示出相当大的聚集无能。