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Multiple acyl-CoA dehydrogenase deficiency (MADD) presenting as polymyositis.

作者信息

Hong Lih En, Phillips Liza K, Fletcher Janice, Limaye Vidya S

机构信息

Rheumatology Department, Royal Adelaide Hospital.

Discipline of Medicine, University of Adelaide.

出版信息

Rheumatology (Oxford). 2020 Dec 1;59(12):e128-e130. doi: 10.1093/rheumatology/keaa348.

DOI:10.1093/rheumatology/keaa348
PMID:32617583
Abstract
摘要

相似文献

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Multiple acyl-CoA dehydrogenase deficiency (MADD) presenting as polymyositis.表现为多发性肌炎的多种酰基辅酶A脱氢酶缺乏症(MADD)。
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Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) Myopathy Misdiagnosed as Polymyositis.迟发性多种酰基辅酶A脱氢酶缺乏症(MADD)肌病被误诊为多发性肌炎。
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Pregnancy of a patient with multiple Acyl-CoA dehydrogenation deficiency (MADD).患有多发性酰基辅酶 A 脱氢酶缺乏症(MADD)的患者怀孕。
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A systematic review of late-onset and very-late-onset multiple acyl-coenzyme A dehydrogenase deficiency: Cohort analysis and patient report from Taiwan.一篇关于迟发性和极迟发性多发性酰基辅酶 A 脱氢酶缺乏症的系统回顾:来自台湾的队列分析和患者报告。
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Adolescent late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting with severe multi-organ failure: a case report.青少年迟发性核黄素反应性多种酰基辅酶A脱氢酶缺乏症伴严重多器官功能衰竭:一例报告
Front Pediatr. 2025 Jul 2;13:1513288. doi: 10.3389/fped.2025.1513288. eCollection 2025.
2
Late-onset multiple acyl-CoA dehydrogenase deficiency: an insidious presentation.迟发性多发性酰基辅酶 A 脱氢酶缺乏症:隐匿性表现。
BMJ Case Rep. 2023 May 22;16(5):e252668. doi: 10.1136/bcr-2022-252668.
3
Late-onset multiple acyl-CoA dehydrogenase deficiency mimicking myositis in an elderly patient: a case report.
迟发性多发性酰基辅酶 A 脱氢酶缺乏症模拟老年患者的肌炎:病例报告。
BMC Neurol. 2020 Dec 2;20(1):436. doi: 10.1186/s12883-020-02010-w.