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患有与脊柱后侧凸相关的埃勒斯-当洛综合征的13岁和10岁兄弟中的自发性腹腔干动脉瘤。

Spontaneous celiac artery aneurysms in 13-year-old and 10-year-old brothers with -related kyphoscoliotic Ehlers-Danlos syndrome.

作者信息

Bhandari Apoorva, Siu Victoria, Duncan Audra A

机构信息

Division of Vascular Surgery, University of Western Ontario, London, ON, Canada.

Division of Medical Genetics, Department of Pediatrics, University of Western Ontario, London, ON, Canada.

出版信息

J Vasc Surg Cases Innov Tech. 2024 Mar 21;10(3):101465. doi: 10.1016/j.jvscit.2024.101465. eCollection 2024 Jun.

Abstract

-related kyphoscoliotic Ehlers-Danlos syndrome is a rare, autosomal recessive connective tissue disorder characterized by congenital hypotonia, early-onset, progressive kyphoscoliosis, and generalized joint hypermobility. -kyphoscoliotic Ehlers-Danlos syndrome is also associated with heightened vascular fragility, resulting in an elevated susceptibility to recurrent vascular complications such as arterial aneurysms, dissection, and spontaneous arterial rupture. We report the cases of two affected brothers: a 13-year-old boy presenting with spontaneous rupture of a celiac artery aneurysm and a 10-year-old boy presenting with a rapidly enlarging celiac artery aneurysm requiring urgent repair.

摘要

与脊柱后侧凸相关的埃勒斯-当洛综合征是一种罕见的常染色体隐性结缔组织疾病,其特征为先天性肌张力减退、早发性进行性脊柱后侧凸和全身关节活动过度。脊柱后侧凸型埃勒斯-当洛综合征还与血管脆性增加有关,导致反复出现血管并发症(如动脉瘤、夹层和自发性动脉破裂)的易感性升高。我们报告了两名患病兄弟的病例:一名13岁男孩出现腹腔动脉动脉瘤自发性破裂,一名10岁男孩出现迅速增大的腹腔动脉动脉瘤,需要紧急修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/11061726/b859786728d7/gr1.jpg

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