Gordon R B, Keough D T, Emmerson B T
J Inherit Metab Dis. 1987;10(1):82-8. doi: 10.1007/BF01799493.
Deficiencies of HPRT are usually associated with increased concentrations of PRPP and increased levels of APRT activity in erythrocytes. We report the case of a male with a partial deficiency of HPRT in whom these two parameters were normal. The clinical features of this patient were those associated with severe hyperuricaemia and gout. Studies of intact erythrocytes showed rates of incorporation of [14C]hypoxanthine and of [14C]adenine into purine nucleotides which were almost indistinguishable from normal. However, HPRT activity in erythrocyte lysates was only 9% of normal. In cell extracts of cultured lymphoblasts, the HPRT activity was 20% of control values and the APRT activity was normal. The PRPP concentration and the rate of de novo purine synthesis in cultured lymphoblasts were both intermediate between controls and lymphoblasts from patients with the Lesch-Nyhan syndrome.
次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(HPRT)缺乏通常与磷酸核糖焦磷酸(PRPP)浓度升高以及红细胞中腺嘌呤磷酸核糖转移酶(APRT)活性水平升高有关。我们报告了一例男性患者,其HPRT部分缺乏,但这两个参数正常。该患者的临床特征与严重高尿酸血症和痛风相关。对完整红细胞的研究表明,[14C]次黄嘌呤和[14C]腺嘌呤掺入嘌呤核苷酸的速率与正常情况几乎没有区别。然而,红细胞裂解物中的HPRT活性仅为正常水平的9%。在培养的淋巴母细胞的细胞提取物中,HPRT活性为对照值的20%,而APRT活性正常。培养的淋巴母细胞中的PRPP浓度和从头嘌呤合成速率均介于对照组和莱施 - 奈恩综合征患者的淋巴母细胞之间。