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Bardet-Biedl syndrome renal transplant and percutaneous nephrolithotomy: a case report and review of the literature

机译:Bardet-Biedl综合征肾移植和经皮肾镜取石术:一例病例并文献复习

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摘要

Bardet-Biedl syndrome is an autosomal recessive disorder with obesity, polydactly, retinitis pigmentosa, hypogenitalism, intellectual impairment and varying degree of renal abnormalities. Fewer than ten cases of paediatric renal transplantation for BBS have been reported in literature so far. This is the only case report of BBS transplant urolithiasis which was dealt with percutaneous nephrolithotomy and has been stone free for seven years. This is a complex case with a rare genetic disorder, renal transplant, renal stone, ileal conduit, long loop and inversely placed kidney. This case exemplifies the need for multidisciplinary management of complex cases and emphasises PCNL as the safe method.
机译:Bardet-Biedl综合征是一种常染色体隐性遗传疾病,具有肥胖,多发性,色素性视网膜炎,性欲减退,智力障碍和不同程度的肾脏异常。迄今为止,文献报道不到十例小儿肾脏BBS移植病例。这是唯一的经BBS移植治疗尿路结石的病例报告,经皮肾镜取石术治疗了7年,无结石。这是一个复杂的病例,有罕见的遗传性疾病,肾移植,肾结石,回肠导管,长环和肾脏倒置。该案例说明了对复杂案例进行多学科管理的必要性,并强调了PCNL是安全的方法。

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