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贝拉尔迪内利-塞普先天性脂肪代谢障碍:一种常染色体隐性疾病,罕见地伴有十二指肠结肠息肉。

Berardinelli-Seip congenital lipodystrophy: an autosomal recessive disorder with rare association of duodenocolonic polyps.

作者信息

Agrawala Ritesh Kumar, Choudhury Arun Kumar, Mohanty Binoy Kumar, Baliarsinha Anoj Kumar

出版信息

J Pediatr Endocrinol Metab. 2014 Sep;27(9-10):989-91. doi: 10.1515/jpem-2013-0399.

Abstract

Berardinelli-Seip congenital lipodystrophy (BSCL) is a rare autosomal recessive disorder characterized by a nearly complete absence of adipose tissue and generalized muscular appearance. This condition is associated with various dermatological and systemic manifestations. We report a 5-year-old boy, with clinical and metabolic presentation resembling BSCL and unusual features, such as diabetes detected at an early age and multiple duodenal and colonic polyps.

摘要

贝拉尔迪内利-塞普先天性脂肪营养不良(BSCL)是一种罕见的常染色体隐性疾病,其特征是几乎完全缺乏脂肪组织并呈现全身性肌肉外观。这种病症与多种皮肤和全身表现相关。我们报告了一名5岁男孩,其临床和代谢表现类似于BSCL,且具有一些不寻常的特征,如早年发现的糖尿病以及多个十二指肠和结肠息肉。

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