论文部分内容阅读
目的:探讨Alport综合征的临床表现,病理学特征及研究进展。方法:分析1例此病患者的临床资料。结果:本例患者临床表现为慢性视力下降。尿常规检查提示蛋白尿,血尿。肾肾穿刺活检的光镜、电镜检查均支持诊断。结论:Alport综合征患者中眼部异常的表现有独特性;了解眼部病变特征并结合全身病史,病理学检查有助于疾病的诊断和随诊。
Objective: To investigate the clinical manifestations, pathological features and research progress of Alport syndrome. Methods: The clinical data of one patient with this disease were analyzed. Results: The clinical manifestations of this patient were chronic vision loss. Urine routine examination prompted proteinuria, hematuria. Renal and renal biopsy light microscopy, electron microscopy are supported by the diagnosis. CONCLUSIONS: Al ocular syndrome patients have unique ocular abnormalities. To understand the characteristics of ocular lesions combined with systemic history, pathological examination is helpful for the diagnosis and follow-up of the disease.