Literature DB >> 23782822

[A case of MELAS with G13513A mutation presenting with chronic kidney disease long before stroke-like episodes].

Atsuko Motoda1, Takashi Kurashige, Tomohito Sugiura, Takeshi Nakamura, Takemori Yamawaki, Koji Arihiro, Masayasu Matsumoto.   

Abstract

The patient was a 35-year-old female with an 9-year history of chronic kidney disease awaiting renal transplantation. She was brought to hospital by ambulance due to a generalized convulsive seizure. Her consciousness remained disturbed after treatment for her seizure, and sensorineural deafness was noted. Lactic acid and pyruvic acid levels were extremely elevated in both the plasma and the cerebrospinal fluid, and brain atrophy was obvious on brain imaging. These findings suggested mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes, which was confirmed by muscle biopsy. Previous renal biopsy specimen showed focal segmental glomerulosclerosis and granular swollen epithelial cells. She had no acute progression of the stroke-like episode with L-arginine treatment. However, the brain lesions expanded on MRI. Mitochondrial DNA analysis from a muscle biopsy specimen showed G13513A mutation. The G13513A mutation and the long history of preceding renal failure before the stroke-like episodes were distinctive features in this case.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23782822     DOI: 10.5692/clinicalneurol.53.446

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN: 0009-918X


  5 in total

1.  Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic Variant.

Authors:  Valentina Barone; Chiara La Morgia; Leonardo Caporali; Claudio Fiorini; Michele Carbonelli; Laura Ludovica Gramegna; Fiorina Bartiromo; Caterina Tonon; Luca Morandi; Rocco Liguori; Aurelia Petrini; Rachele Brugnano; Rachele Del Sordo; Carla Covarelli; Manrico Morroni; Raffaele Lodi; Valerio Carelli
Journal:  Front Genet       Date:  2022-06-03       Impact factor: 4.772

2.  Renal manifestations of primary mitochondrial disorders.

Authors:  Josef Finsterer; Fulvio Alexandre Scorza
Journal:  Biomed Rep       Date:  2017-04-12

Review 3.  Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.

Authors:  Ying-Xin Wang; Wei-Dong Le
Journal:  Chin Med J (Engl)       Date:  2015-07-05       Impact factor: 2.628

4.  Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report.

Authors:  Keiji Sugai; Hiroyuki Ueda; Keita Morimoto; Mai Tanaka; Daisuke Takahashi; Akio Nakashima; Junichiro Kato; Hiroshi Takahashi; Yutaka Yamaguchi; Tetsuya Kawamura; Kazushige Hanaoka; Yoichi Miyazaki; Takashi Yokoo
Journal:  BMC Nephrol       Date:  2018-12-10       Impact factor: 2.388

5.  A MELAS Patient Developing Fatal Acute Renal Failure with Lactic Acidosis and Rhabdomyolysis.

Authors:  Hisashi Ito; Shigeru Fukutake; Sanae Odake; Riki Okeda; Osamu Tokunaga; Tetsumasa Kamei
Journal:  Intern Med       Date:  2020-07-07       Impact factor: 1.271

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.