Chorea triggered by hyperglycemia in a maternally inherited diabetes and deafness (MIDD) patient with the A3243G mutation of mitochondrial DNA and basal ganglia calcification

被引：0
|
作者：
Ji-Hoon Kang
Sa-Yoon Kang
Jay-Chol Choi
Seong-Suk Lee
Ji-Soo Kim
机构：
[1] Cheju National University Hospital,Dept. of Neurology
[2] Cheju National University Hospital,Dept. of Radiology
[3] Seoul National University Bundang Hospital,Dept. of Neurology
来源：
Journal of Neurology | 2005年 / 252卷
关键词：
Public Health; Hyperglycemia; Basal Ganglion; A3243G Mutation; Basal Ganglion Calcification;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：103 / 105
页数：2
相关论文
共 50 条
  • [41] MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD) - A DISTINCT SUBTYPE OF DIABETES-ASSOCIATED WITH A MITOCHONDRIAL TRNA(LEU(UUR)) GENE POINT MUTATION
    VANDENOUWELAND, JMW
    LEMKES, HHPJ
    GERBITZ, KD
    MAASSEN, JA
    [J]. MUSCLE & NERVE, 1995, : S124 - S130
  • [42] The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10-year follow-up observation study and literature review
    Zheng, Shasha
    Wang, Juanjuan
    Sun, Minxian
    Wang, Pei
    Shi, Wei
    Zhang, Zhongzhi
    Wang, Zhongjing
    Zhang, Hongmei
    [J]. CLINICAL CASE REPORTS, 2024, 12 (02):
  • [43] Lack of association between mitochondrial DNA mutation np3243 and maternally inherited diabetes mellitus
    Zambelli, A
    Vidal-Rioja, L
    [J]. CLINICAL BIOCHEMISTRY, 1999, 32 (01) : 81 - 82
  • [44] The level of the mitochondrial mutation A3243G decreases upon ageing in epithelial cells from individuals with diabetes and deafness
    Charlotta Olsson
    Elsy Johnsen
    Mats Nilsson
    Erik Wilander
    Ann-Christine Syvänen
    Maria Lagerström-Fermér
    [J]. European Journal of Human Genetics, 2001, 9 : 917 - 921
  • [45] Screening for the mitochondrial DNA A3243G mutation in children with insulin-dependent diabetes mellitus
    Abad, MM
    Cotter, PD
    Fodor, FH
    Larson, S
    GinsbergFellner, F
    Desnick, RJ
    Abdenur, JE
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1997, 46 (04): : 445 - 449
  • [46] The level of the mitochondrial mutation A3243G decreases upon ageing in epithelial cells from individuals with diabetes and deafness
    Olsson, C
    Johnsen, E
    Nilsson, M
    Wilander, E
    Syvänen, AC
    Lagerström-Fermér, M
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (12) : 917 - 921
  • [47] Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA.: Description of one case
    Biarnés, J
    Barrientos, A
    Ricart, W
    Nunes, V
    Fernández-Castañer, M
    Soler, J
    [J]. MEDICINA CLINICA, 1999, 112 (03): : 99 - 101
  • [48] Maternally inherited diabetes and A3243G mitocondrial mutation in a Brazilian kindred: diagnosis after clinical suspicion in an internal medicine unit
    Frederico Lisboa Nogueira
    Livia Villela Costa
    Nadine Márcia de Faria
    Henry Houlden
    Daniel Dutra Romualdo Silva
    [J]. Diabetology & Metabolic Syndrome, 7 (Suppl 1):
  • [49] Post-treatment retinopathy in a case of diabetes mellitus with A3243G mutation of mitochondrial DNA
    Iwase, M
    Gotoh, D
    Ishibasi, T
    Yoshinari, M
    Fujishima, M
    [J]. JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2001, 15 (03) : 167 - 169
  • [50] Treatment response in the first Emirati patient with diabetes associated with the A3243G mitochondrial point mutation
    Mohammad, A.
    Waheed, N.
    El-Laboudi, A.
    Buckley, A.
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 2022, 186
12345