复发性横纹肌溶解症、急性肾损伤和足下垂：一例罕见的线粒体三功能蛋白（MTP）缺乏症病例 - Suppr

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超能文献

Recurrent Rhabdomyolysis, Acute Kidney Injury, and Foot Drop: A Rare Case with Mitochondrial Trifunctional Protein (MTP) Deficiency.

作者信息

Dabla Surekha, Wangnoo Areca, Kumar Neeraj, Bala Kiran

机构信息

Department of Neurology, Pt. B. D. Sharma University of Health Sciences, Rohtak, Haryana, India.

出版信息

Ann Indian Acad Neurol. 2022 Nov-Dec;25(6):1204-1206. doi: 10.4103/aian.aian_606_22. Epub 2022 Nov 17.

DOI:10.4103/aian.aian_606_22

PMID:36911475

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9996484/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4003/9996484/5274921b5217/AIAN-25-1204-g001.jpg

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引用本文的文献

Foot drop secondary to rhabdomyolysis: improved foot dorsiflexion and gait after neurolysis and distal nerve transfer-a case series and literature review.横纹肌溶解继发足下垂：神经松解术和远端神经移位术后足背屈和步态改善——病例系列及文献综述

J Surg Case Rep. 2023 May 20;2023(5):rjad257. doi: 10.1093/jscr/rjad257. eCollection 2023 May.

本文引用的文献

Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis.线粒体三功能蛋白缺乏症：一种罕见的成人发作性横纹肌溶解症病因。

Muscle Nerve. 2013 Dec;48(6):989-91. doi: 10.1002/mus.23959. Epub 2013 Oct 25.

Mitochondrial fatty-acid oxidation disorders.线粒体脂肪酸氧化障碍

Semin Pediatr Neurol. 2008 Sep;15(3):140-9. doi: 10.1016/j.spen.2008.05.008.

Molecular and phenotypic heterogeneity in mitochondrial trifunctional protein deficiency due to beta-subunit mutations.由于β亚基突变导致的线粒体三功能蛋白缺乏症中的分子和表型异质性。

Hum Mutat. 2003 Jun;21(6):598-607. doi: 10.1002/humu.10211.

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