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

Author:

Ito Hisashi1,Fukutake Shigeru1,Odake Sanae2,Okeda Riki3,Tokunaga Osamu3,Kamei Tetsumasa1

Affiliation:

1. Department of Neurology, Shonan Fujisawa Tokushukai Hospital, Japan

2. Department of Internal Medicine, Sodegaura Satsuki-dai Hospital, Japan

3. Department of Pathology, Shonan Fujisawa Tokushukai Hospital, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Reference13 articles.

1. 1. Sproule DM, Kaufmann P. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome. Ann NY Acad Sci 1142: 133-158, 2008.

2. 2. Klopstock T, Jaksch M, Gasser T. Age and cause of death in mitochondrial diseases. Neurology 53: 855-857, 1999.

3. 3. Ohsawa Y, Hagiwara H, Nishimatsu S, et al. Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial. J Neurol Neurosurg Psychiatry 90: 529-536, 2019.

4. 4. Koenig MK, Emrick L, Karaa A, et al. Recommendations for the management of strokelike episodes in patients with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes. JAMA Neurol 73: 591-594, 2016.

5. 5. Yanagihara C, Oyama A, Tanaka M, Nakaji K, Nishimura Y. An autopsy case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with chronic renal failure. Intern Med 40: 662-665, 2001.

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