1型邓氏病患者母亲活体肾脏捐献

G. Gambaro, A. Naticchia, P. M. Ferraro, G. Spagnoletti, J. Romagnoli, M. P. Salerno, F. Citterio
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引用次数: 2

摘要

邓特病是一种罕见的x连锁隐性疾病,表现在儿童或成年早期,可导致终末期肾脏疾病(ESRD)。它发生在半合子的男性身上。在患有终末期肾病的患者中,一个已故供者的肾脏移植可以治愈这种疾病。雌性是突变基因的专性携带者,有些表现出轻微的登特病表型。在考虑女性义务携带者(即母亲)捐献肾脏时,可能有理由担心肾功能恶化的风险。病例介绍:我们描述了首例成功的肾移植,涉及1型邓特病和ESRD患者,由基因突变的专性携带者,他的母亲给予肾脏。结论:经过对女性专性携带者的仔细评估,家族内肾捐献对1型邓氏病是可行的。供体未见肾功能恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Living Kidney Donation in a Type 1 Dent’s Disease Patient from His Mother
Introduction: Dent’s disease is a rare X-linked recessive disorder that manifests in childhood or early adulthood and can lead to end-stage renal disease (ESRD). It occurs in males, who are hemizygous. In patients who develop ESRD, a deceased donor kidney transplant cures the disease. Females are obligate carriers of the mutated gene, and some show a mild Dent’s disease phenotype. There may be reason for concern when considering a female obligate carrier (i.e., the mother) for kidney donation because of the risk of kidney function deterioration. Case Presentation: We describe the first successful kidney transplantation involving a patient with type 1 Dent’s disease and ESRD given a kidney by an obligate carrier of the gene mutation, his mother. Conclusions: After careful assessment of the female obligate carriers, intrafamilial kidney donation in Dent’s disease type 1 is feasible. No deteriorating renal function in the donor was observed.
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