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伴有肝功能不全的阿尔斯特伦综合征:一例报告。

Alstrom syndrome with hepatic dysfunction: report of one case.

作者信息

Chang K W, Hou J W, Lin S J, Kong M S

机构信息

Department of Pediatric Gastroenterology, Chang Gung Children's Hospital, Taoyuan, Taiwan.

出版信息

Acta Paediatr Taiwan. 2000 Sep-Oct;41(5):270-2.

Abstract

Alstrom syndrome is a rare autosomal recessive disorder associated with early childhood retinopathy, progressive sensorineural hearing loss, truncal obesity, and acanthosis nigricans. We report a 10-year-old boy with Alstrom syndrome presenting with general malaise and abnormal liver function for 1 year. In addition to the above mentioned features, he also had hyperglycemia and hyperinsulinemia. The mechanism responsible for the persistent elevation of liver enzymes could not be identified. To the best of our knowledge, this is the first-reported case of Alstrom syndrome with hepatic dysfunction in Taiwan.

摘要

阿尔斯特伦综合征是一种罕见的常染色体隐性疾病,与儿童早期视网膜病变、进行性感音神经性听力损失、躯干性肥胖和黑棘皮病有关。我们报告一名患有阿尔斯特伦综合征的10岁男孩,出现全身不适和肝功能异常1年。除上述特征外,他还患有高血糖和高胰岛素血症。导致肝酶持续升高的机制尚无法确定。据我们所知,这是台湾首例报告的伴有肝功能障碍的阿尔斯特伦综合征病例。

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