Nogami H, Oohira A, Ozeki K, Oki T, Ogino T, Murachi S
Clin Orthop Relat Res. 1979 Sep(143):251-9.
Ultrastruct of cartilage were examined in Marfan syndrome, Menkes kinky hair syndrome, achondroplasia, asphyxiating thoracic dysplasia, mild diastrophic dysplasia and mucopolysaccharidoses I and III. Ruthenium red staining revealed decrease of proteoglycans in cases with Marfan syndrome and kinky hair syndrome, and increase in cases with osteochondrodysplasia and mucopolysaccharidosis III. This morphologic tendency coincided with the result obtained by biochemical analysis of glycosaminoglycan contents in cartilage matrix from cases with Marfan syndrome (decreased content) and asphyxiating thoracic dysplasia (increased content). It was postulated that proteoglycan content in cartilage matrix might be related to excessive or reduced skeletal growth in Marfan syndrome or osteochondrodysplasia.
对马凡综合征、门克斯卷发综合征、软骨发育不全、窒息性胸廓发育不良、轻度脊柱骨骺发育不良及黏多糖贮积症I型和III型患者的软骨超微结构进行了检查。钌红染色显示,马凡综合征和卷发综合征患者的蛋白聚糖减少,而骨软骨发育不良和黏多糖贮积症III型患者的蛋白聚糖增加。这种形态学趋势与对马凡综合征(含量降低)和窒息性胸廓发育不良(含量增加)患者软骨基质中糖胺聚糖含量进行生化分析的结果一致。据推测,软骨基质中的蛋白聚糖含量可能与马凡综合征或骨软骨发育不良中骨骼过度生长或生长受限有关。