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以极早发病例为重点的儿科女性Leber线粒体视神经病变

Leber Mitochondrial Optic Neuropathy in Pediatric Females With Focus on Very Early Onset Cases.

作者信息

Tagliani Sara, Malaventura Cristina, Ceccato Chiara, Parmeggiani Francesco, Suppiej Agnese

机构信息

Department of Medical Sciences, Pediatric Section, University Hospital of Ferrara, Ferrara, Italy.

87812Robert Hollman Foundation, Padova, Italy.

出版信息

J Child Neurol. 2023 Feb;38(1-2):5-15. doi: 10.1177/08830738221149962. Epub 2023 Jan 19.

Abstract

The aim of this study was to describe the phenotype of Leber hereditary optic neuropathy occurring in pediatric females. This disease generally affects young adult males, but it can occur also in females, and research data in this population is lacking. The very early onset can challenge the diagnosis and delay treatment. We searched PubMed through February 2021 and identified 226 pediatric females with genetically confirmed Leber hereditary optic neuropathy and added a new case of a 3-year-old female. The male-female ratio was 1.8:1; the mean onset age in females was 11 years with the onset at 3 years of age occurring in 3 females only. Acute onset with mild visual impairment was the most common presentation, associated with optic disc edema in 16%. Differential diagnoses are pseudotumor cerebri, optic nerve drusen and optic neuritis. The outcome is poor with partial recovery in 50%, despite some receiving Idebenone therapy.

摘要

本研究的目的是描述发生在儿科女性中的Leber遗传性视神经病变的表型。这种疾病通常影响年轻成年男性,但也可能发生在女性中,而该人群的研究数据匮乏。极早发可能对诊断构成挑战并延误治疗。我们检索了截至2021年2月的PubMed,确定了226例基因确诊的Leber遗传性视神经病变儿科女性,并新增了1例3岁女性病例。男女比例为1.8:1;女性的平均发病年龄为11岁,仅3名女性发病年龄为3岁。急性起病伴轻度视力损害是最常见的表现,16%伴有视盘水肿。鉴别诊断包括假性脑瘤、视神经乳头 drusen和视神经炎。尽管一些患者接受了艾地苯醌治疗,但预后较差,50%的患者部分恢复。

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