Lacasa A, Chabás A, Vera F, Díaz N, Martín N, Tajada N, Gonzalvo N
An Esp Pediatr. 1983 Aug;19(2):118-22.
Authors present a case of mucolipidosis III diagnosed in a boy suffering from articular retractions, platyspondylia and a normal mucolysacchariduria. Biochemical characteristics of the lisosomial enzyme, reduced in fibroblasts in culture and increased in biological fluids allow such diagnose. Primary enzyme lack being not yet explained, authors comment upon the hypothesis trying to explain biochemical findings.
作者报告了一例III型黏脂贮积症病例,该病例为一名患有关节挛缩、扁平椎体且尿黏多糖正常的男孩。溶酶体酶的生化特征在培养的成纤维细胞中减少,而在生物体液中增加,这有助于做出此类诊断。由于原发性酶缺乏尚未得到解释,作者对试图解释生化结果的假说进行了评论。