Twenty-one-year follow-up of variable onset MELAS syndrome with heteroplasmic nt3243A>G mtDNA mutation: A case report-Reference-Cited by-同舟云学术

Twenty-one-year follow-up of variable onset MELAS syndrome with heteroplasmic nt3243A>G mtDNA mutation: A case report

Published:2019-06-30 Issue:1 Volume:16 Page:31-38
ISSN:1226-1769
Container-title:Journal of Genetic Medicine
language:en
Short-container-title:J Genet Med

Author:

Song Wung Joo¹²,Lee Yoon Jin³,Kang Joon Won³,Chang Mea Young³,Song Kyu Sang⁴,Kang Dae Young⁴,Kim Sook Za¹²^ORCID

Affiliation:

1. KSZ Children’s Hospital, Cheongju, Korea

2. Korea Genetics Research Center, Cheongju, Korea

3. Department of Pediatrics, Chungnam National University School of Medicine, Daejeon, Korea

4. Department of Pathology, Chungnam National University School of Medicine, Daejeon, Korea

Publisher

Korean Society of Medical Genetics

Subject

General Medicine

Link

http://pdf.medrang.co.kr/JGM/2019/016/JGM016-01-07.pdf

Reference16 articles.

1. 2001) . MELAS synonyms: mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes; myopathy, mitochondrial-encephalopathy-lactic acidosis-stroke. GeneReviews® [Internet]. [updated 2018 Nov 29; cited 2018 Dec 20]. https://www.ncbi.nlm.nih.gov/books/NBK1233/

2. MELAS: An original case and clinical criteria for diagnosis

3. Late onset of stroke-like episode associated with a 3256C→T point mutation of mitochondrial DNA

4. Late-Onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike Episodes With Bitemporal Lesions

5. Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Patent foramen ovale leading to mismanagement in a mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes patient;Clinical Case Reports;2023-07