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青少年起病的成人型糖尿病一家系报告 被引量:5

Report of a pedigree with patients of maturity onset diabetes of the young
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摘要 青少年起病的成人型糖尿病(maturityonsetdiabetesoftheyoung,MODY)是一种呈常染色体显性遗传特点的单基因突变糖尿病,主要由于胰岛B细胞中葡萄糖刺激的胰岛素分泌缺陷所致。迄今已报道13种MODY亚型,其中MODY5由肝细胞核转录因子1(HNF1β)基因突变引起,临床表型复杂多样,最常见为肾囊肿和糖尿病,又称RCAD综合征(renalcystsanddiabetessyndrome,RCADsyndrome)。本研究针对一个糖尿病合并肝、肾囊肿家系,对其部分成员进行临床分析及基因检测,现报告如下。
出处 《中华内分泌代谢杂志》 CAS CSCD 北大核心 2013年第6期534-535,共2页 Chinese Journal of Endocrinology and Metabolism
基金 基金项目:山东省医学科学院科研基金面上项目(201207)
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  • 1Fujimoto K,Sasaki T,Hiki Y,Nemoto M,Utsunomiya Y,Yokoo T,et al.In vitro and pathological investigations of MODY5 with the R276X-HNF1beta (TCF2) mutation.Endocr J 2007; 54:757-764.
  • 2Karges B,Bergmann C,Scholl K,Heinze E,Rasche FM,Zerres K,et al.Digenic inheritance of hepatocyte nuclear factor-lalpha and -lbeta with maturity-onset diabetes of the young,polycystic thyroid,and urogenital malformations.Diabetes Care 2007; 30:1613-1614.
  • 3Bala V,Anania FA.Increased liver enzyme levels and HNF-1beta gene mutation.Clin Gastroenterol Hepatol 2008; 6:A26.
  • 4Haldorsen IS,Vesterhus M,Raeder H,Jensen DK,Sovik O,Molven A,et al.Lack of pancreatic body and tail in HNF1B mutation carriers.Diabet Med 2008; 25:782-787.
  • 5Hoskins BE,Cramer CH,2nd,Tasic V,Kehinde EO,Ashraf S,Bogdanovic R,et al.Missense mutations in EYA1 and TCF2are a rare cause of urinary tract malformations.Nephrol Dial Transplant 2008; 23:777-779.
  • 6Mayer C,Bottcher Y,Kovacs P,Halbritter J,Stumvoll M.Phenotype of a patient with a de novo mutation in the hepatocyte nuclear factor 1beta/maturity-onset diabetes of theyoung type 5 gene.Metabolism 2008; 57:416-420.
  • 7Thomas CP,Erlandson JC,Edghill EL,Hattersley AT,Stolpen AH.A genetic syndrome of chronic renal failure with multiplerenal cysts and early onset diabetes.Kidney Int 2008; 74:1094-1099.
  • 8Bellanne-Chantelot C,Clauin S,Chauveau D,Collin P,Daumont M,Douillard C,et al.Large genomicrearrangements in the hepatocyte nuclear factor-1beta (TCF2)gene are the most frequent cause of maturity-onset diabetes of the young type 5.Diabetes 2005; 54:3126-3132.
  • 9Muller D,Klopocki E,Neumann LM,Mundlos S,Taupitz M,Schulze I,et al.A complex phenotype with cystic renal disease.Kidney Int 2006; 70:1656-1660.
  • 10Eller P,Kaser S,Lhotta K,Edghill EL,Ellard S,Ebenbichler C,et al.Renal cysts and diabetes due to a heterozygous HNF-1beta gene deletion.Nephrol Dial Transplant 2007; 22:1271-1272.

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  • 1苏莹,陈茜,袁刚,余学锋,何文涛.单基因糖尿病MODY3家系一例[J].临床内科杂志,2022,39(10):709-710. 被引量:2
  • 2钟胜利,束燕雯,顾天伟,毕艳.KCNJ11合并PAX4基因突变致青少年起病的成人型糖尿病家系一例[J].临床内科杂志,2022,39(4):250-252. 被引量:3
  • 3吴静,张素华,倪银星,任伟,李全民.2型糖尿病家系肝细胞核因子1β基因1968A/G的多态性[J].中华糖尿病杂志(1006-6187),2005,13(5):366-367. 被引量:2
  • 4郭振奎,陈刚,晏辉,王天成,栾萌.青少年起病的成人型糖尿病一家系八例[J].中华医学遗传学杂志,2006,23(4):483-483. 被引量:5
  • 5Shields BM, Hicks S, Shepherd MH, et al. Maturity-onset diabetes of the young (MODY). how many cases are we missing? [J]. Diabetologia,2010,53(12).2504-2508.
  • 6Kolatsi-Joannou M, Bingham C, Ellard S, et al. Hepatocyte nuclear factor-lbeta. a new kindred with renal cysts and diabetes and gene expression in normal human development [J]. J Am Soc Nephrol,2001,12(10).2175-2180.
  • 7Lazzaro D, De Simone V, De Magistris L, et al. LFB1 and LFB3 homeoproteins are sequentially expressed during kidney development [J] .Development, 1992, l 14(2).469-479.
  • 8Edghill EL, Bingham C, Ellard S, et al. Mutations in hepatoeyte nuclear factor-113 and their related phenotypes [J]. J Med Genet, 2006,43(1).84-90.
  • 9Lindner TH, Njolstad PR, Horikawa Y, et al. A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-l[3[J]. Hum Mol Genet, 1999,8(11). 2001-2008.
  • 10Okita K, Yang Q, Yamagata K, et al. Human insulin gene is a target gene of hepatoeyte nuclear factor-lalpba (HhF- ltx) and HNF-lJ3[J]. Bioehem Biophys Res Commun,1999,263(2).566- 569.

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