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Subacute Myelopathy: Think Beyond Neuromyelitis Optica Spectrum Disorder.

作者信息

Kasinathan Ananthanarayanan, Suthar Renu, Vyas Sameer, Saini Arushi Gahlot, Sankhyan Naveen, Attri Savita

机构信息

Department of Pediatrics, Mahatma Gandhi Medical College and Research Institute, Puducherry, India.

Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Ann Indian Acad Neurol. 2019 Oct-Dec;22(4):541-542. doi: 10.4103/aian.AIAN_4_19. Epub 2019 Oct 25.

DOI:10.4103/aian.AIAN_4_19
PMID:31736604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6839321/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d32d/6839321/996b01a41e39/AIAN-22-541-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d32d/6839321/996b01a41e39/AIAN-22-541-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d32d/6839321/996b01a41e39/AIAN-22-541-g001.jpg

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引用本文的文献

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Electroclinical Response to a Vitamin: Simple Remedy for a Profound Deficiency.对一种维生素的电临床反应：针对严重缺乏症的简易疗法。
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Visual Loss in Biotinidase Deficiency.

本文引用的文献

1
Clinical utility gene card for: Biotinidase deficiency-update 2015.生物素酶缺乏症临床应用基因卡 - 2015年更新版
Eur J Hum Genet. 2016 Jul;24(7). doi: 10.1038/ejhg.2015.246. Epub 2015 Nov 18.
2
Biotinidase deficiency should be considered in individuals exhibiting myelopathy with or without and vision loss.对于出现脊髓病且伴有或不伴有视力丧失的个体，应考虑生物素酶缺乏症。
Mol Genet Metab. 2015 Nov;116(3):113-8. doi: 10.1016/j.ymgme.2015.08.012. Epub 2015 Sep 3.
3
Biotin and demyelinating diseases--a new connection?
生物素酶缺乏症导致的视力丧失
Ann Indian Acad Neurol. 2020 Nov-Dec;23(6):821. doi: 10.4103/aian.AIAN_503_19. Epub 2019 Dec 19.
4
Metabolic Epilepsy.代谢性癫痫。
Indian J Pediatr. 2021 Oct;88(10):1025-1032. doi: 10.1007/s12098-020-03510-w. Epub 2020 Oct 16.
Mult Scler. 2015 Oct;21(12):1608-9. doi: 10.1177/1352458515599077. Epub 2015 Jul 30.
4
Biotinidase deficiency: "if you have to have an inherited metabolic disease, this is the one to have".生物素酶缺乏症：“如果非得患上一种遗传性代谢疾病，那这种病就是最好的选择”。
Genet Med. 2012 Jun;14(6):565-75. doi: 10.1038/gim.2011.6. Epub 2012 Jan 5.
5
The neurology of biotinidase deficiency.生物素酶缺乏症的神经学表现。
Mol Genet Metab. 2011 Sep-Oct;104(1-2):27-34. doi: 10.1016/j.ymgme.2011.06.001. Epub 2011 Jun 12.
6
Hearing loss is a common feature of symptomatic children with profound biotinidase deficiency.听力损失是有严重生物素酶缺乏症的有症状儿童的一个常见特征。
J Pediatr. 2002 Feb;140(2):242-6. doi: 10.1067/mpd.2002.121938.