Danesino C, Lo Curto F, Bonfant G, Cazzadore C, Voltolin G, Bersi S
Ann Genet. 1984;27(3):162-6.
A patient deficient for most of the short arm of one chromosome 10 is described. The clinical picture is similar to those of other published cases but includes agenesis of olfactory bulbs, an uncommon finding, already noted in few 10p- patients. The normal levels of hexokinase 1 found in the fibroblasts of the patient allow a more precise localization of the gene at band 10p11.2. The results obtained for inorganic pyrophosphatase confirm the data available from two other cases.
本文描述了一名10号染色体一条短臂大部分缺失的患者。临床表现与其他已发表病例相似,但包括嗅球发育不全,这是一种罕见的发现,在少数10p-患者中已有报道。在该患者成纤维细胞中发现的己糖激酶1水平正常,这使得该基因能更精确地定位在10p11.2带。无机焦磷酸酶的检测结果证实了另外两个病例的数据。