Martinelli B, Campailla E
Ital J Orthop Traumatol. 1975 Apr;1(1):141-50.
The authors present three cases of dyschondrosteosis occurring in a single family unit. The characteristics of the "major" and "minor" forms of this genetically derived chondrosteodysplasia are described. The other members of the family examined presented no signs of the disease, but they were very young. The possibility of successful surgical correction of the deformities caused by dyscondrosteosis is stressed.
作者报告了一个家族中出现的三例先天性软骨发育不全症病例。描述了这种遗传性软骨骨发育不良的“主要”和“次要”形式的特征。接受检查的家族其他成员未表现出该病的症状,但他们都非常年轻。强调了成功手术矫正先天性软骨发育不全症所致畸形的可能性。