A rare condition that mimic myopathy: Late-onset glutaric acidaemia type II-Reference-Cited by-同舟云学术

A rare condition that mimic myopathy: Late-onset glutaric acidaemia type II

Published:2023-09-01 Issue:3 Volume:4 Page:173-175
ISSN:2719-4523
Container-title:Rheumatology and Immunology Research
language:en
Short-container-title:

Author:

Liu Jianwen¹,Wu Chenmin¹,Gao Fei¹,Yan Qing¹^ORCID

Affiliation:

1. Department of Rheumatology and Immunology, Fujian Provincial Hospital, Shengli Clinical Medical College of Fujian Medical University , Fuzhou , Fujian province , China

Publisher

Walter de Gruyter GmbH

Subject

General Medicine

Link

https://www.degruyter.com/document/doi/10.2478/rir-2023-0026/pdf

Reference9 articles.

1. Prasad M, Hussain S. Glutaric aciduria type II presenting as myopathy and rhabdomyolysis in a teenager. J Child Neurol. 2015;30:96–99.

2. Hong D, Yu Y, Wang Y, Xu Y, Zhang J. Acute-onset multiple acyl-CoA dehydrogenase deficiency mimicking Guillain-Barré syndrome: two cases report. BMC Neurol. 2018;18:219.

3. Koca M, Erden A, Armagan B, et al. Two cases of glutaric aciduria type II: how to differentiate from inflammatory myopathies? Acta Clin Belg. 2019;74:451–455.

4. Yamada K, Kobayashi H, Bo R, et al. Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases. Brain Dev. 2016;38:293–301.

5. Prasun P. Multiple Acyl-CoA Dehydrogenase Deficiency. 2020 Jun 18. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022.

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