Stellamor K, Anzböck W
Zentralröntgeninstitut Krankenanstalt Rudolfstiftung der Stadt Wien.
Rontgenblatter. 1989 Oct;42(10):437-40.
A case of a fully developed hereditary onycho-osteo-arthrodysplasia (nail-patella syndrome) is presented. The typical signs, such as the iliac horns or variations of the knees, cubitals and nails should be familiar to every radiologist. The associated nephropathy seems to be caused by typical changes in the glomerular basement membrane seen in electron microscopy. Asymptomatic proteinuria is found in about 60% of the cases, in 5.5-8% the disease leads to the necessity of haemodialysis because of renal insufficiency. Hence, early diagnosis is very important.
本文报告一例完全发展型遗传性甲髌综合征(遗传性指甲-髌骨发育不良)。髂骨角或膝、肘及指甲的变异等典型体征,每位放射科医生都应熟悉。相关肾病似乎是由电子显微镜下所见肾小球基底膜的典型变化引起的。约60%的病例出现无症状蛋白尿,5.5%-8%的病例因肾功能不全导致需要进行血液透析。因此,早期诊断非常重要。