荷兰糖尿病人群中母系遗传糖尿病和耳聋的患病率。 - Suppr

Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands.

作者信息

t Hart L M, Lemkes H H, Heine R J, Stolk R P, Feskens E J, Jansen J J, van der Does F E, Grobbee D E, Kromhout D, van den Ouweland J M

出版信息

Diabetologia. 1994 Nov;37(11):1169-70. doi: 10.1007/BF00418385.

DOI:10.1007/BF00418385

PMID:7867892

Abstract

摘要

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Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands.荷兰糖尿病人群中母系遗传糖尿病和耳聋的患病率。

Diabetologia. 1994 Nov;37(11):1169-70. doi: 10.1007/BF00418385.

Prevalence of maternally inherited diabetes and deafness in Australian diabetic subjects.澳大利亚糖尿病患者中母系遗传糖尿病和耳聋的患病率。

Diabetologia. 1999 Aug;42(8):1028-9. doi: 10.1007/s001250051264.

Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.由线粒体DNA 3243 tRNA（Leu）A到G突变引起的色素性视网膜营养不良以及母系遗传糖尿病和耳聋综合征。

Ophthalmology. 1999 Jun;106(6):1101-8. doi: 10.1016/S0161-6420(99)90244-0.

Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.线粒体糖尿病：日本患者中线粒体tRNA（Leu（UUR））基因突变所致糖尿病的患病率及临床特征

Diabetologia. 1994 May;37(5):504-10. doi: 10.1007/s001250050139.

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.母系遗传的糖尿病和耳聋是糖尿病的一种独特亚型，与线粒体tRNA（Leu（UUR））基因中的单点突变有关。

Diabetes. 1994 Jun;43(6):746-51. doi: 10.2337/diab.43.6.746.

Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.母系遗传的糖尿病和耳聋（MIDD）：一种与线粒体tRNA（Leu）（UUR）基因点突变相关的独特糖尿病亚型。

Muscle Nerve Suppl. 1995;3:S124-30. doi: 10.1002/mus.880181425.

Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group.母系遗传糖尿病和耳聋中黄斑图案营养不良的患病率。GEDIAM研究小组。

Ophthalmology. 1999 Sep;106(9):1821-7. doi: 10.1016/s0161-6420(99)90356-1.

[Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA. Apropos a case].[与线粒体DNA A3243G突变相关的糖尿病。关于一例病例]

Med Clin (Barc). 1999 Jan 30;112(3):99-101.

Non-isotopic and sensitive method for diagnosis of maternally-inherited diabetes and deafness.母系遗传糖尿病和耳聋诊断的非同位素敏感方法。

Diabetologia. 1994 Aug;37(8):842. doi: 10.1007/BF00404343.

Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.一个患有母系遗传II型糖尿病和耳聋的大家系中线粒体tRNA(Leu)(UUR)基因的突变

Nat Genet. 1992 Aug;1(5):368-71. doi: 10.1038/ng0892-368.

引用本文的文献

Endocrine disorders in mitochondrial disease.线粒体疾病中的内分泌紊乱。

Mol Cell Endocrinol. 2013 Oct 15;379(1-2):2-11. doi: 10.1016/j.mce.2013.06.004. Epub 2013 Jun 13.

Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELAS.线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）中mtDNA A3243G突变负荷的纵向变化及功能水平

Am J Med Genet A. 2009 Feb 15;149A(4):584-7. doi: 10.1002/ajmg.a.32703.

Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence.通过眼底自发荧光对携带A3243G线粒体DNA点突变患者的黄斑营养不良进行特征描述。

Br J Ophthalmol. 2008 May;92(5):623-9. doi: 10.1136/bjo.2007.131177.

Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.糖尿病患者血液中线粒体tRNALeu（UUR）3243A>G低水平突变的检测

Mol Diagn Ther. 2006;10(6):381-9. doi: 10.1007/BF03256215.

Mitochondrial diabetes mellitus.线粒体糖尿病

J Endocrinol Invest. 2002 May;25(5):477-84. doi: 10.1007/BF03344042.

Deficiency of phosphofructo-1-kinase/muscle subtype in humans impairs insulin secretion and causes insulin resistance.人类中磷酸果糖-1-激酶/肌肉亚型的缺乏会损害胰岛素分泌并导致胰岛素抵抗。

J Clin Invest. 1997 Dec 1;100(11):2833-41. doi: 10.1172/JCI119831.

Maternally inherited diabetes and deafness: a new diabetes subtype.母系遗传的糖尿病和耳聋：一种新的糖尿病亚型。

Diabetologia. 1996 Apr;39(4):375-82. doi: 10.1007/BF00400668.

A mutation in the glucagon receptor gene (Gly40Ser): heterogeneity in the association with diabetes mellitus.胰高血糖素受体基因的一种突变（甘氨酸40丝氨酸）：与糖尿病关联的异质性

Diabetologia. 1995 Aug;38(8):983-5. doi: 10.1007/BF00400589.

本文引用的文献

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.一种与线粒体DNA突变相关的糖尿病亚型。

N Engl J Med. 1994 Apr 7;330(14):962-8. doi: 10.1056/NEJM199404073301403.

Diabetologia. 1994 May;37(5):504-10. doi: 10.1007/s001250050139.

Diabetes. 1994 Jun;43(6):746-51. doi: 10.2337/diab.43.6.746.

Prevalence of mitochondrial gene mutations in families with diabetes mellitus.糖尿病家族中线粒体基因突变的患病率。

Lancet. 1993 Dec 4;342(8884):1429-30. doi: 10.1016/0140-6736(93)92792-r.

[Hypothalamic GH Deficiency and gelastic seizures in a 10-year-old girl with MELAS].[一名患有线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）的10岁女孩的下丘脑生长激素缺乏症和痴笑性癫痫]

No To Hattatsu. 1991 Jul;23(4):411-6.

Nat Genet. 1992 Aug;1(5):368-71. doi: 10.1038/ng0892-368.

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Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands.

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