扩大MEGDEL综合征的流行病学和表型谱:来自埃及的第一例报告。

IF 1.2 Q2 PEDIATRICS
Clinical Medicine Insights-Pediatrics Pub Date : 2025-08-14 eCollection Date: 2025-01-01 DOI:10.1177/11795565251348345
Abdelrahim A Sadek, Mohammed A Aladawy, Tarek Mm Mansour, Mohammed Fawzy Fouad, Rofaida M Magdy, Mohamed Mohamed Elmoursy, Elsayed Abdelkreem
{"title":"扩大MEGDEL综合征的流行病学和表型谱:来自埃及的第一例报告。","authors":"Abdelrahim A Sadek, Mohammed A Aladawy, Tarek Mm Mansour, Mohammed Fawzy Fouad, Rofaida M Magdy, Mohamed Mohamed Elmoursy, Elsayed Abdelkreem","doi":"10.1177/11795565251348345","DOIUrl":null,"url":null,"abstract":"<p><p>MEGDEL syndrome is a rare autosomal recessive disease characterized by 3-methylglutaconic aciduria, deafness-dystonia, hepatopathy, encephalopathy, and leigh-like syndrome, which results from biallelic pathogenic variants in <i>SERAC1</i> gene. The diagnosis is commonly challenging due to the diverse clinical manifestations. Herein, we report the first case of MEGDEL syndrome from the Egyptian population. This is a 7-year-old boy born to first cousins Arab parents from Egypt with family history of unexplained deaths of 3 siblings during the neonatal period. He presented with developmental regression since the age of 2 years resulting in marked muscle weakness with no head support, generalized spasticity more prominent in lower limbs, and aphonia, but intact hearing. The child had excessive urinary excretion of 3-methylglutaconic acid, and his brain magnetic resonance imaging showed characteristic basal ganglia affection with \"Putaminal eye sign.\" Whole-exome sequencing demonstrated a likely pathogenic homozygous c.1404-2A>G variant in <i>SERAC1</i> gene. This report expands the epidemiological and phenotypic spectrum of MEGDEL syndrome by reporting the first case from the Egyptian population who had relatively delayed onset and no evident hepatopathy or deafness.</p>","PeriodicalId":45027,"journal":{"name":"Clinical Medicine Insights-Pediatrics","volume":"19 ","pages":"11795565251348345"},"PeriodicalIF":1.2000,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12354997/pdf/","citationCount":"0","resultStr":"{\"title\":\"Expanding the Epidemiological and Phenotypic Spectrum of MEGDEL Syndrome: The First Case Report From Egypt.\",\"authors\":\"Abdelrahim A Sadek, Mohammed A Aladawy, Tarek Mm Mansour, Mohammed Fawzy Fouad, Rofaida M Magdy, Mohamed Mohamed Elmoursy, Elsayed Abdelkreem\",\"doi\":\"10.1177/11795565251348345\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>MEGDEL syndrome is a rare autosomal recessive disease characterized by 3-methylglutaconic aciduria, deafness-dystonia, hepatopathy, encephalopathy, and leigh-like syndrome, which results from biallelic pathogenic variants in <i>SERAC1</i> gene. The diagnosis is commonly challenging due to the diverse clinical manifestations. Herein, we report the first case of MEGDEL syndrome from the Egyptian population. This is a 7-year-old boy born to first cousins Arab parents from Egypt with family history of unexplained deaths of 3 siblings during the neonatal period. He presented with developmental regression since the age of 2 years resulting in marked muscle weakness with no head support, generalized spasticity more prominent in lower limbs, and aphonia, but intact hearing. The child had excessive urinary excretion of 3-methylglutaconic acid, and his brain magnetic resonance imaging showed characteristic basal ganglia affection with \\\"Putaminal eye sign.\\\" Whole-exome sequencing demonstrated a likely pathogenic homozygous c.1404-2A>G variant in <i>SERAC1</i> gene. This report expands the epidemiological and phenotypic spectrum of MEGDEL syndrome by reporting the first case from the Egyptian population who had relatively delayed onset and no evident hepatopathy or deafness.</p>\",\"PeriodicalId\":45027,\"journal\":{\"name\":\"Clinical Medicine Insights-Pediatrics\",\"volume\":\"19 \",\"pages\":\"11795565251348345\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2025-08-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12354997/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Medicine Insights-Pediatrics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/11795565251348345\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"PEDIATRICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Medicine Insights-Pediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/11795565251348345","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

摘要

MEGDEL综合征是一种罕见的常染色体隐性遗传病,以3-甲基戊二酸尿症、耳聋-肌痉挛障碍、肝病、脑病和leigh样综合征为特征,由SERAC1基因双等位基因致病变异引起。由于临床表现多样,诊断通常具有挑战性。在这里,我们报告的第一例MEGDEL综合征从埃及人口。这是一个7岁的男孩,父母是来自埃及的阿拉伯表兄妹,在新生儿时期有3个兄弟姐妹不明原因死亡的家族史。他自2岁起出现发育倒退,导致明显的肌肉无力,无头部支撑,下肢全身性痉挛更突出,失音,但听力完好。患儿尿中3-甲基戊二酸排泄过多,脑磁共振显示特征性基底节区病变,伴有“膜眼征”。全外显子组测序显示SERAC1基因可能存在致病性纯合子c.1404-2A >g变异。本报告通过报告埃及人群中发病相对延迟且无明显肝病或耳聋的第一例病例,扩大了MEGDEL综合征的流行病学和表型谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expanding the Epidemiological and Phenotypic Spectrum of MEGDEL Syndrome: The First Case Report From Egypt.

MEGDEL syndrome is a rare autosomal recessive disease characterized by 3-methylglutaconic aciduria, deafness-dystonia, hepatopathy, encephalopathy, and leigh-like syndrome, which results from biallelic pathogenic variants in SERAC1 gene. The diagnosis is commonly challenging due to the diverse clinical manifestations. Herein, we report the first case of MEGDEL syndrome from the Egyptian population. This is a 7-year-old boy born to first cousins Arab parents from Egypt with family history of unexplained deaths of 3 siblings during the neonatal period. He presented with developmental regression since the age of 2 years resulting in marked muscle weakness with no head support, generalized spasticity more prominent in lower limbs, and aphonia, but intact hearing. The child had excessive urinary excretion of 3-methylglutaconic acid, and his brain magnetic resonance imaging showed characteristic basal ganglia affection with "Putaminal eye sign." Whole-exome sequencing demonstrated a likely pathogenic homozygous c.1404-2A>G variant in SERAC1 gene. This report expands the epidemiological and phenotypic spectrum of MEGDEL syndrome by reporting the first case from the Egyptian population who had relatively delayed onset and no evident hepatopathy or deafness.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
5
审稿时长
8 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信