戴克-戴维多夫-马森综合征--一个病例系列

S. Sheetal, Joel Varghese Sujan, Athira Das, Vivek Mathai
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引用次数: 0

摘要

戴克-戴维多夫-马森综合征(Dyke-Davidoff-Masson Syndrome,DDMS)是指由于宫内或出生后早期的脑损伤导致的一侧大脑半球不同程度的萎缩。这种罕见综合征的临床特征包括不同程度的对侧偏瘫、面部不对称、癫痫发作和智力低下。具体的神经影像学检查结果包括单侧脑容量减少、脑室肥大和代偿性骨肥大。此外,还可能出现颅骨增厚和额窦过度充气。我们在此报告了三例该综合征的病例,其临床和影像学特征各不相同,以突出该综合征的广泛性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dyke–Davidoff–Masson Syndrome – A Case Series
Dyke–Davidoff–Masson syndrome (DDMS) refers to variable degrees of atrophy of one cerebral hemisphere, resulting from brain injury in intrauterine or early years of life. Clinical features of this rare syndrome include varying degrees of contralateral hemiplegia, facial asymmetry, seizures, and mental retardation. Specific neuroimaging findings include unilateral brain volume loss, ventriculomegaly, and compensatory bone hypertrophy. In addition to this, calvarial thickening and hyperpneumatization of frontal sinuses may occur. We hereby report three cases of this syndrome, with varied clinical and radiographic features, to highlight the wide spectrum of this syndrome.
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