Crossan J F, Wynne-Davies R, Fulford G E
J Pediatr Orthop. 1983 Jul;3(3):297-301. doi: 10.1097/01241398-198307000-00005.
A radiographic survey of 25 patients with bilateral Perthes disease is compared with four inherited skeletal dysplasias also affecting the hip joints (45 patients with multiple epiphyseal dysplasia, 22 with spondyloepiphyseal dysplasia tarda, 18 with pseudoachondroplasia, and 17 with spondyloepiphyseal dysplasia congenita). The distinguishing features in relation to the pelvis and hip joint in the growing child are ascertained, in view of the importance of differentiating as early as possible the transient disorder of Perthes disease from the more serious progressive disorders.
对25例双侧佩特兹病患者进行了影像学检查，并与另外四种同样累及髋关节的遗传性骨骼发育不良疾病（45例多发性骨骺发育不良患者、22例迟发性脊椎骨骺发育不良患者、18例假性软骨发育不全患者和17例先天性脊椎骨骺发育不良患者）进行了比较。鉴于尽早将佩特兹病的短暂性病症与更严重的进行性病症区分开来的重要性，确定了在成长中的儿童中与骨盆和髋关节相关的鉴别特征。
