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Classic Triad of Ross Syndrome with Diffuse Ay tonomic Dysfunction and Positive Antinuclear Antibody Titre

机译:罗斯综合征的经典三联征,弥漫性Ay机能障碍和阳性抗核抗体滴度

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摘要

A 23-year-old woman presented with left-sided hemifacial flushing and hyperhidrosis with right-sided anhi-drosis. Examination showed a dilated right pupil and a slightly constricted left pupil with bilateral sluggish vermiform movements and light-near dissociation. A neurological examination showed absent deep tendon reflexes. Magnetic resonance imaging of the brain, neck, and spine was normal. These features are consistent with Ross syndrome. Ross syndrome is characterized by Holmes-Adie syndrome (tonic pupil, areflexia of deep tendon reflexes) and segmental anhidrosis and lies within the spectrum of peripheral, partial autonomic dysfunction syndromes together with harlequin and Homer syndromes. In addition to the classic triad of Ross syndrome, the patient had diffuse, systemic autonomic dysfunction with a positive antinuclear antibody test and a positive ribonucleoprotein antibody titre.
机译:一名23岁妇女出现左侧半面部潮红和多汗症并伴有右侧无汗症。检查显示右瞳孔散大,左瞳孔略微收缩,双侧ver状运动迟缓,轻度分离。神经系统检查显示无深部肌腱反射。脑,颈部和脊柱的磁共振成像正常。这些特征与罗斯综合征一致。罗斯综合症的特征是霍姆斯-阿迪综合症(强直性瞳孔,深部肌腱反射性反射消失)和节段性多汗症,并且属于周围性,部分自主神经功能障碍综合症以及丑角和荷马综合症。除罗斯综合征的经典三联征外,患者还患有弥漫性系统性自主神经功能障碍,抗核抗体试验阳性,核糖核蛋白抗体滴度阳性。

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