Kondoh T, Matsumoto T, Ochi M, Sukegawa K, Tsuji Y
Department of Pediatrics, Nagasaki University School of Medicine, Japan.
J Hum Genet. 1998;43(1):59-61. doi: 10.1007/s100380050038.
We used magnetic resonance imaging (MRI) to examine the brain of a typical Coffin-Lowry syndrome (CLS) patient. There were many small perivascular focal areas of hypointensity in the white matter on T1-weighted images, similar to those found in mucopolysaccharidosis or perivascular leukomalacia. However, these changes could not seen in another patient we examined. Both patients showed normal urinary mucopolysaccharide patterns with chromatographic analysis. The cause of the MRI result is not known, but it could have a heterogeneous origin, and this result could represent an important indication defining one type of CLS.
我们使用磁共振成像(MRI)对一名典型的科芬-洛里综合征(CLS)患者的脑部进行了检查。在T1加权图像上,白质中有许多小的血管周围局灶性低信号区,类似于黏多糖贮积症或血管周围白质软化症中发现的区域。然而,在我们检查的另一名患者中未发现这些变化。两名患者的尿黏多糖色谱分析结果均正常。MRI结果的原因尚不清楚,但可能有多种来源,这一结果可能是定义一种CLS类型的重要指征。