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Cardio-facio-cutaneous syndrome and moyamoya syndrome.

机译:心脏-面部皮肤综合症和烟雾病综合症。

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We reported a patient with cardio-facio-cutaneous (CFC) syndrome associated with moyamoya syndrome. The patient was referred at 6 years 5 months with left hemiplegia and right-sided eye deviation. He had an apparently short stature, macrocephaly, left ptosis and atopic skin, and was odd looking. He exhibited an incomplete right bundle branch block on electrocardiogram and an atrial septal defect on ultrasound cardiography. He was diagnosed as having CFC syndrome. Head magnetic resonance imaging showed a flow void in the bilateral basal ganglia, but did not show any ischemic changes. Magnetic resonance angiography showed bilateral stenosis with an internal carotid artery at the Willis artery ring level and bilateral moyamoya. Contrast angiography demonstrated occlusion of both middle cerebral arteries. Cerebrovascular anomalies have not previously been reported in CFC syndrome. This is the first case of CFC syndrome associated with moyamoya syndrome.
机译:我们报道了一名与烟雾病综合征相关的心-皮肤-皮肤(CFC)综合征患者。该患者在6年5个月时因左偏瘫和右眼偏斜转诊。他的身材矮小,大头畸形,左眼下垂和特应性皮肤,看上去很奇怪。他在心电图上表现出不完全的右束支传导阻滞,在超声心动图上表现出房间隔缺损。他被诊断出患有CFC综合征。头部磁共振成像显示双侧基底神经节有血流空洞,但未显示任何缺血性变化。磁共振血管造影显示双侧狭窄,在威利斯动脉环水平处有颈内动脉和双侧烟雾病。造影造影显示两个大脑中动脉闭塞。先前在CFC综合征中尚未报道过脑血管异常。这是与Moyamoya综合征相关的CFC综合征的首例病例。

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