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卵磷脂-胆固醇酰基转移酶缺乏肾病一例 被引量:1

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摘要 卵磷脂-胆固醇酰基转移酶(lecithin - cholesterolacyltransferase, LCAT)缺乏肾病为临床罕见病,临床表现为蛋白尿及肾功能减退,容易误诊为原发性肾小球肾炎,现将1例卵磷脂.胆固醇酰基转移酶缺乏相关肾病病例汇报如下,通过文献复习,旨在提高对该病认识。
作者 刘涛
出处 《中华肾脏病杂志》 CAS CSCD 北大核心 2015年第10期790-792,共3页 Chinese Journal of Nephrology
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参考文献12

  • 1Qu Sl, Fan HZ, Blanco - Vaca F, et al. In vitro expression of natural mutants of human lecithin:cholesterol acyltransferase[l]. 1 Lipid Res, 1995,36(5): 967-974. 被引量:1
  • 2Funke H, von Eckardstein A, Pritchard PH, et al. Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease[J]. J Clin Invest, 1993,91(2): 677-683. 被引量:1
  • 3Idzior- Walus B. Familial LCAT deficiency[l]. Przegl Lek, 2001, 58(10): 919-923. 被引量:1
  • 4Scarpioni R, Paties C, Bergonzi G. Dramatic atherosclerotic vascular burden in a patient with familial lecithin - cholesterol acyltransferase (LCAT) deficiency [J]. Nephrol Dial Transplant, 2008, 23(3): 1074-1075 . 被引量:1
  • 51ahanzad I, Amoueian S, Attaranzadeh A. Familial lecithincholesterol acyltransferase deficiency[J]. Arch Iran Med, 2009,12 (2): 179-181. 被引量:1
  • 6Lager DJ, Rosenberg BF, Shapiro H, et al. Lecithin cholesterol acyltransferase deficiency: ultrastructural examination of sequential renal biopsies[J]. Mod Pathol, 1991,4(3): 331-335. 被引量:1
  • 7Takahashi S, Hiromura K, Tsukida M, et al. Nephrotic syndrome caused by immune - mediated acquired LCAT deficieney[l]. 1 Am Soc Nephrol, 2013, 24(8): 1305-1312. 被引量:1
  • 8Strem EH, Sund S, Reier-Nilsen M, et al. Lecithin: Cholesterol Acyltransferase (LeA T) Deficiency: renal lesions with early graft recurrence[J]. Ultrastruct Pathol, 2011, 35(3): 139-145. 被引量:1
  • 9Stockenbroek RM, van den Bergh Weerman MA, Hovingh GK, et al. Familial LCAT deficiency: from renal replacement to enzyme replacement [J]. Neth J Med, 2013, 71(1): 29-31. 被引量:1
  • 10张庭廷,夏晓凯.卵磷脂胆固醇酰基转移酶缺乏综合征[J].生命的化学,1999,19(6):294-296. 被引量:4

二级参考文献34

  • 1张小瑛,崔若兰,李霖,李闻捷.改良的LCAT测定及其在肾脏疾病中的临床意义[J].肾脏病与透析肾移植杂志,1995,4(4):318-319. 被引量:4
  • 2Jahanzad I,Amoueian S,Attaranzadeh A.Familial lecithin-cholesterol acyltransferase deficiency[J].Arch Iran Med,2009,12(2):179-81. 被引量:1
  • 3Idzior-Walu B,Sieradzki J,Rostworowski W,et al.Familial LCAT deficiency-clinical picture[J].Pol Arch Med Wewn,2000,104 (3):591-6. 被引量:1
  • 4Scarpioni R,Paties C,Bergonzi G.Dramatic atherosclerotic vascular burden in a patient with familial lecithin-cholesterol acyltransferase (LCAT) deficiency[J].Nephrol Dial Transplant.2008,23(3):1074-5. 被引量:1
  • 5Li Min,Biochem Biophys Acta,1998年,1391卷,2期,256页 被引量:1
  • 6Kuivenhoven JA, Pritchard H, Hill J, et al.The molecular pathology of lecithin : cholesterol acyhransferase ( LCAT ) deficiency syndromes. J Lipid Res, 1997,38 (2) : 191-205. 被引量:1
  • 7Shoji K, Morita H, Ishigaki Y, et al. Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence : a case report and literature review. Clin Nephrol, 2011,76 (4) :323-328. 被引量:1
  • 8Li M, Kuivenhoven JA, Ayyobi AF, et al. T→ G or T→A mutation introduced in the branchpoint consensus sequence of intron 4 of lecithin : cholesterol aeyltransferase ( LCAT ) gene : intron retention causing LCAT deficiency. Biochim Biophys Acta, 1998, 1391 (2) :256-264. 被引量:1
  • 9Frase~t GM,Soverini L, Tampieri E, et al.A 33-year-old man with nephrotie syndrome and lecithin-cholesterol aeyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene. Nephrol Dial Transplant,2004,19(6) : 1622-1624. 被引量:1
  • 10Gjone E, Blomhoff JP, Skarbovik AJ. Possible association between an abnormal low density lipoprotein and nephropathy in lecithin: cholesterol aeyltransferase deficieney.Cliniea Chimica Aeta, 1974,54 (1) :11-8. 被引量:1

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