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首页> 外文期刊>American journal of medical genetics, Part A >Recurrent compartment syndrome in a patient with clinical features of a connective tissue disorder
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Recurrent compartment syndrome in a patient with clinical features of a connective tissue disorder

机译:具有结缔组织疾病临床特征的患者复发室综合征

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摘要

Arterial complications are common in vascular type Ehlers-Danlos syndrome (EDS), accounting for 66% of first complications. Several cases in the literature have documented acute compartment syndrome (ACS) following vascular rupture in vascular type EDS. Other disorders of connective tissue have also demonstrated vascular fragility, leading to arterial aneurysm and rupture, but there have been no documented cases of ACS. Here, we report on a female patient with a history of recurrent compartment syndrome who exhibits some clinical findings seen in hypermobile and vascular EDS; however she does not meet clinical and molecular diagnostic criteria for either of them. We further review the literature on ACS in heritable connective tissue disorders and suggest that compartment syndrome may rarely complicate other heritable disorders of connective tissue.
机译:血管并发症在血管型Ehlers-Danlos综合征(EDS)中很常见,占首次并发症的66%。文献中有几例文献报道了血管性EDS血管破裂后的急性室综合征(ACS)。其他结缔组织疾病也表现出血管脆弱性,导致动脉瘤和破裂,但尚无ACS病例记录。在此,我们报道了一位女性患者,该患者具有复发性室综合征的病史,该病患者在超活动性和血管性EDS中表现出一些临床发现。但是她都不符合任何一项的临床和分子诊断标准。我们进一步回顾了关于ACS在可遗传性结缔组织疾病中的文献,并提示隔室综合征可能很少使其他可遗传性结缔组织疾病复杂化。

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