Advanced Clinical Research Center, Institute for Neurological Disorders, Fukushima and Kanagawa, Japan.
Mol Genet Metab. 2013 Nov;110(3):401-4. doi: 10.1016/j.ymgme.2013.08.006. Epub 2013 Aug 17.
Niemann-Pick disease type C (NP-C) is an autosomal recessive lysosomal lipid storage disorder characterized with accumulation of cholesterol in endosomes and lysosomes. The diagnosis of NP-C is difficult due to its heterogeneous group of diseases. Biochemical diagnosis of NP-C is conducted by cholesterol staining with cultured skin fibroblasts and confirmed by the analysis of genetic mutations of NPC1 or NPC2 gene. Here, we report an easier biochemical diagnostic method with blood smear by filipin staining.
尼曼-匹克病 C 型(NP-C)是一种常染色体隐性溶酶体脂质贮积病,其特征是在内体和溶酶体中胆固醇蓄积。由于 NP-C 疾病的异质性,其诊断较为困难。NP-C 的生化诊断通过培养的皮肤成纤维细胞进行胆固醇染色,并通过 NPC1 或 NPC2 基因突变分析来确认。在此,我们报告了一种更简单的血液涂片 Filipin 染色生化诊断方法。