A nationwide survey of Vici syndrome in Japan.

IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY
Ikumi Hori, Toshihiko Iwaki, Emi Sato, Daisuke Ieda, Yutaka Negishi, Ayako Hattori, Shinji Saitoh
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引用次数: 0

Abstract

Background: Vici syndrome (VICIS) is a congenital disorder characterized by agenesis of the corpus callosum, cataracts, hypopigmentation, cardiomyopathy, combined immunodeficiency, microcephaly, and failure to thrive. This study aimed to elucidate the number of patients with VICIS, its clinical characteristics and relevant genetic information in Japan.

Methods: After developing diagnostic criteria for VICIS, we conducted a nationwide questionnaire-based survey of VICIS in Japan. In the initial survey, we investigated the number of VICIS patients who fulfilled definite or probable criteria. The second survey was used to obtain detailed clinical and genetic information of VICIS from institutions that responded to the initial survey.

Results: Clinical information was available for 15 patients (12 definite, three probable). As of October 2023, nine patients (60%) were alive and six (40%) had died. All patients presented with developmental delay, agenesis of the corpus callosum, elevated serum aspartate/alanine aminotransferase, hypopigmentation and hypotonia. Developmental delay was profound. Most patients developed recurrent infection, high-arched palate, epilepsy, failure to thrive, and microcephaly. Cardiomyopathy and cataracts, both initially described as principal features in VICIS, were notably uncommon in our study. Based on the information collected, all 14 patients for whom information was available received home medical care: 11 (79%) received tube feeding, three (21%) required noninvasive ventilation, four (29%) required tracheostomy, and four (29%) required home subcutaneous immunoglobulin administration.

Conclusion: This study revealed for the first time the nationwide status of patients with VICIS in Japan. The mortality rate of patients with VICIS is as high as 40%, and almost all VICIS patients require various forms of home medical care, necessitating comprehensive management. Additionally, we identified one adult patient, underscoring the need for comprehensive medical management extending into adulthood for patients with VICIS.

日本维西综合征全国调查。
背景介绍维奇综合征(VICIS)是一种先天性疾病,以胼胝体发育不全、白内障、色素沉着、心肌病、联合免疫缺陷、小头畸形和发育不良为特征。本研究旨在阐明日本 VICIS 患者的人数、临床特征和相关遗传信息:方法:在制定了 VICIS 诊断标准后,我们在日本全国范围内对 VICIS 进行了问卷调查。在首次调查中,我们调查了符合明确或可能标准的 VICIS 患者人数。第二次调查是为了从对初次调查做出回应的机构获得 VICIS 的详细临床和遗传信息:结果:共获得 15 名患者(12 名确诊,3 名可能)的临床信息。截至 2023 年 10 月,9 名患者(60%)存活,6 名患者(40%)死亡。所有患者均表现为发育迟缓、胼胝体发育不全、血清天冬氨酸/丙氨酸氨基转移酶升高、色素沉着和肌张力低下。发育严重迟缓。大多数患者会出现反复感染、高腭、癫痫、发育不良和小头畸形。最初被描述为 VICIS 主要特征的心肌病和白内障在我们的研究中并不常见。根据收集到的信息,14 名患者均接受了家庭医疗护理:11 人(79%)接受了管饲,3 人(21%)需要无创通气,4 人(29%)需要气管造口术,4 人(29%)需要家庭皮下注射免疫球蛋白:本研究首次揭示了日本全国 VICIS 患者的状况。VICIS患者的死亡率高达40%,几乎所有VICIS患者都需要各种形式的家庭医疗护理,因此必须进行综合管理。此外,我们还发现了一名成年患者,这凸显了对成年 VICIS 患者进行全面医疗管理的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Brain & Development
Brain & Development 医学-临床神经学
CiteScore
3.60
自引率
0.00%
发文量
153
审稿时长
50 days
期刊介绍: Brain and Development (ISSN 0387-7604) is the Official Journal of the Japanese Society of Child Neurology, and is aimed to promote clinical child neurology and developmental neuroscience. The journal is devoted to publishing Review Articles, Full Length Original Papers, Case Reports and Letters to the Editor in the field of Child Neurology and related sciences. Proceedings of meetings, and professional announcements will be published at the Editor''s discretion. Letters concerning articles published in Brain and Development and other relevant issues are also welcome.
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