Giugliani R, Ferrari I, Greene L J
Urology. 1986 Jan;27(1):38-40. doi: 10.1016/0090-4295(86)90203-7.
Occasional urine samples from 200 stone-forming individuals were screened by the successive application of the cyanide-nitroprusside test, qualitative-semiquantitative thin-layer amino acid chromatography, and quantitative ion-exchange amino acid analysis to determine the frequency of cystinuria in this region of Brazil. Only 1 homozygous cystinuria patient was detected, a lower frequency than 1 to 6 per cent reported in other countries. The patient's family showed a I/I genotype. Since 6 heterozygotes for cystinuria +/II or +/III were also detected, the relative rarity of homozygotes in this sample supports the view of the relatively greater contribution of etiologic factors other than gene frequency to stone formation. The importance of diagnosis based on quantitative amino acid analysis is emphasized because of the different therapeutic and prognostic implications of the homozygote and heterozygote forms of the disease.
通过连续应用氰化高铁氰化物试验、定性 - 半定量薄层氨基酸色谱法和定量离子交换氨基酸分析法,对来自200名结石形成个体的随机尿液样本进行筛查,以确定巴西该地区胱氨酸尿症的发病率。仅检测到1例纯合子胱氨酸尿症患者,其发病率低于其他国家报道的1%至6%。该患者家族显示为I/I基因型。由于还检测到6例胱氨酸尿症+/II或+/III的杂合子,该样本中纯合子相对罕见,这支持了除基因频率外,其他病因因素对结石形成贡献相对更大的观点。由于该疾病纯合子和杂合子形式具有不同的治疗和预后意义,因此强调了基于定量氨基酸分析进行诊断的重要性。