Mak B S, Chi C S, Tsai C R, Lee W J, Lin H Y
Department of Pediatrics, Taichung Veterans General Hospital;, Taichung, Taiwan.
Pediatr Neurol. 2000 Oct;23(4):332-5. doi: 10.1016/s0887-8994(00)00199-5.
Lesch-Nyhan syndrome is an X-linked recessive disorder involving the purine metabolism, with resultant hyperuricemia, choreoathetosis, self-mutilation, and profound neurologic dysfunction. A deficiency of the enzyme hypoxanthine guanine phosphoribosyl-transferase is responsible for the disease. The human HPRT gene is located at Xq26-27 and consists of 57 base pairs. At least 2,000 mutations throughout the HPRT gene coding region from exon 1-9 have been reported. Four patients from three Chinese families were diagnosed with Lesch-Nyhan syndrome according to the clinical and laboratory findings. DNA studies revealed the first family (Patients 1 and 2) had a missense mutation in exon 3 of the HPRT encoding region. This novel mutation occurs in the hot spot of the HPRT gene. The second family (Patient 3) was found to have a missense mutation in exon 8 of the HPRT gene. The third family (Patient 4) carried a mutation in the splicing region of intron 4 of the HPRT gene. All three mutations were de novo.
莱施-奈恩综合征是一种与嘌呤代谢有关的X连锁隐性疾病,会导致高尿酸血症、舞蹈手足徐动症、自残行为以及严重的神经功能障碍。次黄嘌呤鸟嘌呤磷酸核糖转移酶缺乏是该疾病的病因。人类HPRT基因位于Xq26 - 27,由57个碱基对组成。据报道,在整个HPRT基因编码区(外显子1 - 9)至少有2000种突变。根据临床和实验室检查结果,来自三个中国家庭的四名患者被诊断为莱施-奈恩综合征。DNA研究显示,第一个家庭(患者1和2)在HPRT编码区外显子3有一个错义突变。这种新突变发生在HPRT基因的热点区域。第二个家庭(患者3)在HPRT基因外显子8发现有错义突变。第三个家庭(患者4)在HPRT基因内含子4的剪接区域有一个突变。这三种突变均为新发突变。