Congenital CD59 Deficiency-A Novel Cause of Relapsing-Remitting Polyneuropathy.
作者信息
Cornelius Leema P, Livingston Jered, Elango Neeraj
机构信息
Department of Paediatric Neurology, Institute of Child, Health and Hospital for Children, Madras Medical College, Chennai, Tamil Nadu, India.
出版信息
Ann Indian Acad Neurol. 2025 Jul 1;28(4):604-605. doi: 10.4103/aian.aian_1084_24. Epub 2025 Jul 16.
Abstract
摘要
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本文引用的文献
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Inherited CD59 deficiency, where neurology and genetics intertwine.遗传性 CD59 缺陷：神经与遗传相互交织。
Neurosciences (Riyadh). 2023 Apr;28(2):130-135. doi: 10.17712/nsj.2023.2.20220119.
2
Optic neuritis in CD59 deficiency: an extremely rare presentation.CD59 缺乏症中的视神经炎：一种极其罕见的表现。
Turk J Pediatr. 2022;64(4):787-794. doi: 10.24953/turkjped.2021.1405.
3
CD59 deficiency presenting as polyneuropathy and Moyamoya syndrome with endothelial abnormalities of small brain vessels.CD59 缺乏症表现为多发性神经病和伴有小脑血管内皮异常的烟雾病。
Eur J Paediatr Neurol. 2018 Sep;22(5):870-877. doi: 10.1016/j.ejpn.2018.04.003. Epub 2018 Apr 13.
4
Neonatal-Onset Recurrent Guillain-Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency.新生儿起病的复发性吉兰-巴雷综合征样疾病：遗传性CD59缺乏症的线索
Neuropediatrics. 2017 Dec;48(6):477-481. doi: 10.1055/s-0037-1604483. Epub 2017 Aug 11.
5
Demyelination, strokes, and eculizumab: Lessons from the congenital CD59 gene mutations.脱髓鞘、中风与依库珠单抗：先天性CD59基因突变的教训
Mol Immunol. 2017 Sep;89:69-72. doi: 10.1016/j.molimm.2017.05.024. Epub 2017 Jun 13.
6
Paroxysmal nocturnal hemoglobinuria (PNH) and primary p.Cys89Tyr mutation in CD59: Differences and similarities.阵发性睡眠性血红蛋白尿症（PNH）与CD59基因原发性p.Cys89Tyr突变：异同点
Mol Immunol. 2015 Sep;67(1):51-5. doi: 10.1016/j.molimm.2015.03.005. Epub 2015 Mar 26.
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N Engl J Med. 2014 Jan 2;370(1):90-2. doi: 10.1056/NEJMc1308104.
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