MIDD and MELAS: A Clinical Spectrum
Author:
Affiliation:
1. Department of Neurology, Institute of Neurological Sciences, Tottori University Faculty of Medicine
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
http://www.jstage.jst.go.jp/article/internalmedicine/44/4/44_4_276/_pdf
Reference8 articles.
1. 1) Maassen JA. Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis. Am J Med Genet 115: 66-70, 2002.
2. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
3. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
4. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
5. 5) Iizuka T, Sakai F, Endo M, Suzuki N. Response to sumatriptan in headache of MELAS syndrome. Neurology 61: 577-578, 2003.
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3. Maternally inherited diabetes and deafness (MIDD) syndrome with m.3243A>G mutation associated with renal failure — a case report;Clinical Diabetology;2020-12-30
4. MITOCHONDRIAL CYTOPATHIES: MELAS AND MIDD SYNDROMES. ONE GENETIC DEFECT - DIFFERENT CLINICAL APPEARANCES;The Neurological Journal;2017
5. Low prevalence of patients with mitochondrial disease in the German/Austrian DPV diabetes registry;European Journal of Pediatrics;2015-12-15
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