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Multiple Vitelliform Lesions as a Retinal Manifestation of Alport Syndrome

机译:多发性弓形病变是Alport综合征的视网膜表现。

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摘要

Alport syndrome is associated with various ocular phenotypic features, including several retinal manifestations. The purpose of this case report was to describe a case of multiple vitelliform lesions in Alport syndrome. This particular finding has, to our knowledge, not been reported previously. A 63-year-old man with known Alport syndrome presented with symptomatic, bilateral anterior lenticonus. Fundoscopic examination revealed multiple vitelliform lesions, which were symmetrically distributed at the posterior poles. Additional retinal findings included an irregular foveal contour and central macular thinning in both eyes, as well as a multilayered retinoschisis in the left eye. The underlying pathophysiology of the vitelliform lesions may be a dysfunctional Bruch's membrane.
机译:Alport综合征与多种眼表型特征有关,包括几种视网膜表现。本病例报告的目的是描述Alport综合征中的多个玻璃样病变的病例。据我们所知,这一特殊发现以前没有被报道过。一名患有Alport综合征的63岁男子出现症状性双侧前突突。眼底镜检查发现多个玻璃状病变,在后极对称分布。额外的视网膜发现包括两只眼睛的凹凹轮廓不规则和黄斑中央变薄,以及左眼的多层视网膜分裂症。玻璃状病变的潜在病理生理可能是功能失调的布鲁赫膜。

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