Nakamura K, Kurokawa T, Nagano A, Nakamura S, Taniguchi K, Hamazaki M
Department of Orthopedic Surgery, Faculty of Medicine, University of Tokyo, Japan.
Am J Med Genet. 1997 Oct 3;72(1):11-7.
Dyggve-Melchior-Clausen syndrome without mental retardation (Smith-McCort dysplasia) (SM) has clinical and radiographic findings similar to those of Dyggve-Melchior-Clausen syndrome (DMC) except for mental retardation. Iliac crest biopsies from two patients with SM were examined. The lace-like appearance of the iliac crests, which is a characteristic radiological sign of SM and DMC, was caused by bone tissue deposited in a wavy pattern at the osteochondral junction. The growth plate showed abnormal enchondral ossification with no columnarization of chondrocytes. Electron microscopy demonstrated chondrocytes with dilated cisternae of rough endoplasmic reticulum containing fine granular or amorphous material, similar to those reported in cases of DMC. Thus, SM has pathologic changes in common with DMC as a rough endoplasmic reticulum storage disorder, even though the mental condition is different.
无智力发育迟缓的迪格维-梅尔基奥尔-克劳森综合征(史密斯-麦科特发育异常)(SM)具有与迪格维-梅尔基奥尔-克劳森综合征(DMC)相似的临床和影像学表现,但无智力发育迟缓。对两名SM患者的髂嵴活检组织进行了检查。髂嵴的花边样外观是SM和DMC的特征性放射学表现,它是由骨组织以波浪状沉积于骨软骨交界处所致。生长板显示软骨内骨化异常,软骨细胞无柱状排列。电子显微镜显示软骨细胞的粗面内质网池扩张,含有细颗粒状或无定形物质,与DMC病例中报道的情况相似。因此,尽管智力状况不同,但作为一种粗面内质网储存障碍,SM与DMC具有共同的病理变化。