Andrés A, Praga M, Ruilope L M, Martínez J M, Millet V G, Bello I, Rodicio J L
Nephron. 1987;46(2):179-81. doi: 10.1159/000184337.
A 12-year-old boy presented with acute renal failure (ARF) accompanied by a disproportionate increase of serum uric acid level and massive uric acid crystalluria. After alkalinization and allopurinol therapy, serum uric acid and renal function returned to normal values. A further enzymatic study showed the existence of a partial hypoxanthine-guanine phosphoribosyl transferase (HPRT) deficit (less than 1% of HPRT normal activity). Although ARF is an exceptional form of presentation of HPRT deficiency, this possibility should be considered whenever an ARF is accompanied by disproportionate high levels of serum uric acid.
一名12岁男孩出现急性肾衰竭(ARF),伴有血清尿酸水平不成比例升高和大量尿酸结晶尿。经过碱化和别嘌呤醇治疗后,血清尿酸和肾功能恢复到正常水平。进一步的酶学研究显示存在部分次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(HPRT)缺陷(低于HPRT正常活性的1%)。虽然ARF是HPRT缺乏症的一种罕见表现形式,但只要ARF伴有不成比例的高血清尿酸水平,就应考虑这种可能性。