Van Calcar S C, Harding C O, Lyne P, Hogan K, Banerjee R, Sollinger H, Rieselbach R E, Wolff J A
Waisman Center, University of Wisconsin-Madison, USA.
J Inherit Metab Dis. 1998 Oct;21(7):729-37. doi: 10.1023/a:1005493015489.
Renal insufficiency is frequently reported in mutase-deficient methylmalonic acidaemia. We present a case report of a patient with mut- methylmalonic acidaemia who developed chronic tubulointerstitial nephropathy during adolescence. At 24 years of age, she developed end-stage renal failure and underwent renal transplantation. Both plasma and urine methylmalonic acid levels decreased significantly with improved renal function following transplantation. Complications included cyclosporin toxicity and development of diabetes. Renal, metabolic, and clinical status remained improved at 3 years after the kidney transplant.
在甲基丙二酸血症 mutase 缺乏型中,肾功能不全经常被报道。我们报告一例 mut - 甲基丙二酸血症患者,其在青春期发生了慢性肾小管间质性肾病。24岁时,她发展为终末期肾衰竭并接受了肾移植。移植后随着肾功能改善,血浆和尿液中的甲基丙二酸水平显著下降。并发症包括环孢素毒性和糖尿病的发生。肾移植3年后,肾脏、代谢和临床状况持续改善。