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Parry Romberg syndrome with a wide range of ocular manifestations: a case report

机译:帕里·罗姆伯格综合征(Parry Romberg syndrome)具有多种眼部表现:一例病例报告

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Background Parry-Romberg syndrome (PRS) is a rare disorder characterized by unilateral facial atrophy affecting the skin, subcutaneous tissue, muscles, and sometimes extending to the osteocartilaginous structures. Ocular involvement is relatively rare. Case presentation We present a case of a 23-year-old female caucasian patient with Parry Romberg syndrome and extensive ocular involvement: enophthalmos, uveitis, iris atrophy. Ultrasound biomicroscopy (UBM) demonstrated hypotrophy of the ciliary body. The ciliary body atrophy has been previously reported just once and can be an explanation for the hypotony, frequently present in these patients. Conclusions Parry Romberg syndrome is a rare multidisciplinary disease. Our case presents a full spectrum of ocular manifestations. The pathogenesis of hypotonia is discussed.
机译:背景Parry-Romberg综合征(PRS)是一种罕见的疾病,其特征是单侧面部萎缩会影响皮肤,皮下组织,肌肉,有时会延伸至骨软骨结构。眼部受累相对较少。病例介绍我们介绍了一例23岁的帕里·罗姆贝格综合症且广泛的眼部受累的女性白种人患者:眼睑,葡萄膜炎,虹膜萎缩。超声生物显微镜检查(UBM)显示睫状体营养不良。睫状体萎缩以前仅报道过一次,可以解释这些患者中经常出现的肌张力低下。结论Parry Romberg综合征是一种罕见的多学科疾病。我们的病例显示了全范围的眼部表现。讨论了肌张力低下的发病机理。

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