A Mother and a Child with Maternally Inherited Diabetes and Deafness (MIDD) Showing Atrophy of the Cerebrum, Cerebellum and Brainstem on Magnetic Resonance Imaging (MRI)
Author:
Affiliation:
1. Department of Neurology
2. Endocrine-Metabolism, Musashino Redcross Hospital
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
http://www.jstage.jst.go.jp/article/internalmedicine/44/4/44_4_328/_pdf
Reference10 articles.
1. 1) Suzuki S, Oka Y, Kadowaki T, et al. Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A-G) mutation in Japanese: maternal inheritance and mitochondria-related complications. Diabetes Res Clin Pract 59: 207-217, 2003.
2. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
3. 3) Chinnery PF, Schon EA. Mitochondria. J Neurol Neurosurg Psychiatry 74: 1188-1199, 2003.
4. 4) Guillausseau PJ, Massin P, Dubois-LaForgue D, et al. Maternally inherited diabetes and deafness: a multicenter study. Ann Intern Med 134: 721-728, 2001.
5. 5) Suzuki Y, Hata T, Miyaoka H, et al. Diabetes with the 3243 mitochondrial tRNALeu(UUR) mutation. Characteristic neuroimaging findings. Diabetes Care 19: 739-743, 1996.
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