Strøm E H, Strømme P, Westvik J, Pedersen S J
Department of Pathology, Ullevål Hospital, Oslo, Norway.
Pediatr Nephrol. 1993 Jun;7(3):253-5. doi: 10.1007/BF00853211.
The carbohydrate-deficient glycoprotein (CDG) syndrome is a newly described genetic disorder with autosomal recessive inheritance and multiple organ involvement. We describe five patients with the CDG syndrome who all had abnormal renal structure. In two patients autopsy disclosed multiple microcysts. A hyperechogenic pattern strongly suggesting microcysts was demonstrated in all patients that were available for ultrasound examination, while a large single cyst was also seen in one patient. Based on these findings and the reports of others, renal cysts appear to be common in the CDG syndrome.
糖基化缺陷糖蛋白(CDG)综合征是一种新描述的常染色体隐性遗传且累及多器官的遗传性疾病。我们描述了5例患有CDG综合征的患者,他们均有肾脏结构异常。2例患者尸检发现多个微囊肿。所有接受超声检查的患者均显示出强烈提示微囊肿的高回声模式,同时1例患者还可见一个大的单发性囊肿。基于这些发现及其他报告,肾囊肿在CDG综合征中似乎很常见。