首页> 外文期刊>Neuro-ophthalmology >Facial Dystonia with Facial Grimacing and Vertical Gaze Palsy with 'Round the Houses' Sign in a 29-Year-Old Woman
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Facial Dystonia with Facial Grimacing and Vertical Gaze Palsy with 'Round the Houses' Sign in a 29-Year-Old Woman

机译:面部肌张力障碍和面部凝视和垂直凝视麻痹与“环绕房屋”标志着一名29岁的妇女

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A 29-year-old woman developed progressive dysarthria and coordination problems from the age of 15. Examination showed dysarthria, facial dystonia, bibrachial dystonia, hyperreflexia, ataxia, and emotional incontinence. Downward supranuclear gaze palsy was prominent with a "Round the Houses" sign. Magnetic resonance imaging of the brain and medulla, eiectroneurography, and cerebrospinal fluid were normal. A computed tomography scan showed hepatosplenomegaly. This combination of progressive neurological symptoms together with hepatosplenomegaly was suggestive of inborn error of metabolism. A bone marrow biopsy showed an increased number of macrophages with foamy content, highly suggestive of lysosomal disease. Plasmatic chitotriosidase activity and CCL18 were increased. Genetic testing showed heterozygosis for the variation C.1070CW (p.Ser357Leu) and C.1843HT (Arg615Cys), confirming the diagnosis of Niemann-Pick type C (NPC). The "Round the Houses" sign has only been described in patients with progressive supranuclear palsy (PSP). This sign is described as an inability to produce pure vertical saccades along the midline and instead moving the eyes in a lateral arc to accomplish the movement. The observation of this sign in a patient with NPC indicates that this bedside finding is not specific for PSP, but a sign of medial longitudinal fasciculus dysfunction. The presence of facial dystonia with facial grimacing together with supranuclear gaze palsy is highly characteristic and useful for the diagnosis of NPC. NPC is an important underdiagnosed condition, given the availability of treatment and a mean diagnostic delay of 6 years.
机译:一名29岁的妇女从15岁开始出现进行性构音障碍和协调障碍,检查发现构音障碍,面部肌张力障碍,双臂肌张力障碍,反射亢进,共济失调和情绪失禁。向下的核上凝视麻痹突出,并带有“ Round the Houses”标志。脑和髓质的磁共振成像,脑电图和脑脊液均正常。计算机断层扫描显示肝脾肿大。进行性神经系统症状与肝脾肿大的结合提示先天性代谢错误。骨髓活检显示巨噬细胞数量增多,泡沫丰富,高度提示溶酶体病。血浆壳三糖苷酶活性和CCL18增加。遗传学测试显示C.1070CW(p.Ser357Leu)和C.1843HT(Arg615Cys)变异具有杂合性,证实了Niemann-Pick C型(NPC)的诊断。仅在进行性核上性麻痹(PSP)的患者中描述了“房屋周围”标志。这种迹象被描述为无法沿中线产生纯垂直扫视,而无法使眼睛沿侧向弧线移动以完成运动。在NPC患者中观察到这种体征表明,该床旁发现并非PSP特有,而是内侧纵筋膜功能障碍的体征。面部肌张力障碍伴面部鬼脸以及核上凝视麻痹的存在具有很高的特征性,可用于诊断NPC。鉴于可获得的治疗方法和平均6年的诊断延迟,NPC是一种重要的未被诊断的疾病。

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