Alroy Joseph, Pfannl Rolf, Slavov Dobromir, Taylor Matthew R G
Department of Pathology, Tufts University, Cummings Veterinary School, Boston, Massachusetts, USA.
Ultrastruct Pathol. 2010 Dec;34(6):333-6. doi: 10.3109/01913123.2010.499024.
Danon disease is a rare lysosomal disorder. It is due to deficiency of lysosomal-associated protein-2. In human LAMP-2 gene is located at chromosome region Xq24. Danon disease is characterized by hypertrophic cardiomyopathy, skeletal myopathy, mental retardation and retinopathy. To date, the morphological characterization of Danon disease has been limited to endomyocardial and skeletal muscle biopsies. In the current study we demonstrated that electron microscopy of a more accessible tissue, skin biopsies, is a useful method in the diagnosis of Danon disease.
丹侬病是一种罕见的溶酶体疾病。它是由于溶酶体相关蛋白-2缺乏所致。在人类中,LAMP-2基因位于X染色体区域Xq24。丹侬病的特征是肥厚性心肌病、骨骼肌病、智力发育迟缓及视网膜病。迄今为止,丹侬病的形态学特征仅限于心内膜和骨骼肌活检。在本研究中,我们证明了对更容易获取的组织——皮肤活检进行电子显微镜检查,是诊断丹侬病的一种有用方法。