Hartsfield J K, Kousseff B G
University of South Florida College of Medicine, Department of Pediatrics, Tampa 33612-4799.
Am J Med Genet. 1990 Dec;37(4):465-70. doi: 10.1002/ajmg.1320370408.
An 18-year-old Caucasian woman has been followed since age 12 years for Ehlers-Danlos syndrome (EDS) with easy bruisability and "cigarette paper scars." Her chief complaint at age 17 years was tooth mobility, especially in the anterior mandible, necessitating the removal of the four incisors. Initial biochemical analysis of cultured skin fibroblasts indicated the presence of pepsin-sensitive type III collagen. Subsequent analysis of cultured skin fibroblasts by the same laboratory and another laboratory found no abnormality in the type III collagen with or without protease treatment. This is in distinction to the finding of abnormal type III collagen in the only two reported patients with EDS and early-onset periodontitis who have had collagen analyses. One of them was diagnosed as EDS type IV and the other as EDS type VIII, although the defects of type III collagen were consistent with EDS type IV. The defect in type III collagen in some patients with early periodontitis and the considerable overlap of the clinical manifestations of EDS types IV and VIII point out the need for further studies of collagen formation and maturation in any patient who has early periodontitis and who has been classified with EDS type IV or VIII.
一名18岁的白种女性自12岁起就因患有埃勒斯-当洛综合征(EDS)而接受随访,她有易瘀伤和“香烟纸样瘢痕”的症状。她17岁时的主要诉求是牙齿松动,尤其是下颌前部的牙齿,因此不得不拔除了四颗门牙。对培养的皮肤成纤维细胞进行的初步生化分析表明存在对胃蛋白酶敏感的III型胶原蛋白。同一实验室和另一个实验室随后对培养的皮肤成纤维细胞进行分析,发现无论有无蛋白酶处理,III型胶原蛋白均无异常。这与仅有的两例报告的患有EDS和早发性牙周炎且进行了胶原蛋白分析的患者中发现的III型胶原蛋白异常情况不同。其中一例被诊断为IV型EDS,另一例为VIII型EDS,尽管III型胶原蛋白的缺陷与IV型EDS一致。一些早发性牙周炎患者的III型胶原蛋白缺陷以及IV型和VIII型EDS临床表现的大量重叠表明,对于任何患有早发性牙周炎且被归类为IV型或VIII型EDS的患者,都需要进一步研究胶原蛋白的形成和成熟过程。