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MELAS Syndrome and MIDD Unmasked by Metformin Use: A Case Report.

作者信息

Kim Na Hyun, Siddiqui Mahrukh, Vogel Jonathan

机构信息

Amita Health Saint Joseph Hospital, Chicago, Illinois (N.H.K., M.S., J.V.).

出版信息

Ann Intern Med. 2021 Jan;174(1):124-125. doi: 10.7326/L20-0292. Epub 2020 Aug 25.

DOI:10.7326/L20-0292
PMID:32833489
Abstract
摘要

相似文献

1
MELAS Syndrome and MIDD Unmasked by Metformin Use: A Case Report.二甲双胍使用后揭示的线粒体脑肌病伴乳酸血症和卒中样发作综合征及母系遗传糖尿病伴耳聋:一例报告
Ann Intern Med. 2021 Jan;174(1):124-125. doi: 10.7326/L20-0292. Epub 2020 Aug 25.
2
[A clinical case of mitochondrial diabetes].[线粒体糖尿病临床病例]
Rev Med Liege. 2014 Jan;69(1):12-5.
3
One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation.一种突变,三种表型:m.3243A>G 突变导致的 MELAS、MIDD 和肌病的新代谢见解。
Metabolomics. 2021 Jan 12;17(1):10. doi: 10.1007/s11306-020-01769-w.
4
MIDD or MELAS : that's not the question MIDD evolving into MELAS : a severe phenotype of the m.3243A>G mutation due to paternal co-inheritance of type 2 diabetes and a high heteroplasmy level.线粒体糖尿病(MIDD)或线粒体脑肌病伴乳酸血症和卒中样发作(MELAS):这不是问题所在。MIDD演变为MELAS:由于2型糖尿病的父系共同遗传和高异质性水平导致的m.3243A>G突变的严重表型。
Neth J Med. 2012 Dec;70(10):460-2.
5
A novel mutation in mitochondrial DNA in a patient with diabetes, deafness and proteinuria.一名患有糖尿病、耳聋和蛋白尿患者的线粒体DNA发生新型突变。
Neth J Med. 2016 Dec;74(10):455-457.
6
mTOR inhibitors may benefit kidney transplant recipients with mitochondrial diseases.mTOR 抑制剂可能有益于患有线粒体疾病的肾移植受者。
Kidney Int. 2019 Feb;95(2):455-466. doi: 10.1016/j.kint.2018.08.038. Epub 2018 Nov 22.
7
Diabetes and nephrotic syndrome: Answers.糖尿病与肾病综合征:答案
Pediatr Nephrol. 2017 Oct;32(10):1887-1889. doi: 10.1007/s00467-016-3560-9. Epub 2016 Dec 23.
8
Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report.母系遗传糖尿病伴耳聋合并系膜区半乳糖缺乏 IgA1 沉积:病例报告。
BMC Nephrol. 2018 Dec 10;19(1):350. doi: 10.1186/s12882-018-1152-6.
9
Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.成人线粒体疾病中风样发作期间及发作后氨基酸谱的动态紊乱:一例报告
J Med Case Rep. 2019 Oct 21;13(1):313. doi: 10.1186/s13256-019-2255-9.
10
Vacant mitochondria in the myocardium of a patient with mitochondrial cardiomyopathy and diabetes mellitus.一名患有线粒体心肌病和糖尿病患者心肌中的空泡化线粒体。
BMJ Case Rep. 2012 Aug 8;2012:bcr2012006645. doi: 10.1136/bcr-2012-006645.

引用本文的文献

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Precision treatment of beta-cell monogenic diabetes: a systematic review.β细胞单基因糖尿病的精准治疗:一项系统综述
Commun Med (Lond). 2024 Jul 18;4(1):145. doi: 10.1038/s43856-024-00556-1.
2
A case of exacerbated encephalopathy with stroke-like episodes and lactic acidosis triggered by metformin in a patient with MELAS.MELAS 患者因二甲双胍引发的伴有类似中风样发作和乳酸性酸中毒的恶化性脑病病例。
Neurol Sci. 2024 May;45(5):2337-2339. doi: 10.1007/s10072-024-07343-9. Epub 2024 Jan 24.
3
Endocrine features of primary mitochondrial diseases.
原发性线粒体疾病的内分泌特征。
Curr Opin Endocrinol Diabetes Obes. 2024 Feb 1;31(1):34-42. doi: 10.1097/MED.0000000000000848. Epub 2023 Dec 4.
4
Systematic Review of Treatment of Beta-Cell Monogenic Diabetes.β细胞单基因糖尿病治疗的系统评价
medRxiv. 2023 Sep 22:2023.05.12.23289807. doi: 10.1101/2023.05.12.23289807.
5
Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report.延误诊断线粒体脑肌病、乳酸酸中毒和卒中样发作(MELAS)综合征患者,表现为癫痫持续状态和乳酸酸中毒:病例报告。
J Med Case Rep. 2022 Oct 10;16(1):361. doi: 10.1186/s13256-022-03613-2.
6
Macular findings expedite accurate diagnosis of MIDD in a young female patient with newly diagnosed diabetes.黄斑病变表现有助于快速准确诊断一名新诊断糖尿病年轻女性患者的线粒体糖尿病伴耳聋(MIDD)。
Am J Ophthalmol Case Rep. 2022 May 7;27:101578. doi: 10.1016/j.ajoc.2022.101578. eCollection 2022 Sep.
7
Case Report: Late-Onset Mitochondrial Disease Uncovered by Metformin Use in a Patient With Acute Verbal Auditory Agnosia.病例报告:二甲双胍治疗引发急性言语听觉失认症患者迟发性线粒体疾病
Front Neurol. 2022 Mar 25;13:863047. doi: 10.3389/fneur.2022.863047. eCollection 2022.
8
The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.母系遗传糖尿病和耳聋中的突变和临床变异性:161 例患者分析。
Front Endocrinol (Lausanne). 2021 Nov 25;12:728043. doi: 10.3389/fendo.2021.728043. eCollection 2021.