Mauriac Syndrome in a Patient of Type 1 Diabetes Mellitus

Nandita Bagchi, Rashmi N. Nagdeve, Abhishek Walke, S. Chatterjee
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Abstract

Mauriac syndrome is a metabolic complication of poor glycaemic control in Type 1 DM patients, unique to children, characterised by growth failure, short stature, delayed puberty, Cushingoid features, and marked hepatomegaly from massive deposition of glycogen. It is probably due to a combination of factors including inadequate glucose uptake and utilisation in the tissues, decreased insulin-like growth factor-1 and growth hormone levels, impaired bioactivity of these hormones, a circulating hormone inhibitor, resistant or defective hormone receptors, insulin deficiency, and poor glycaemic control. This syndrome is rarely seen nowadays because of better treatment modalities.
1型糖尿病患者的毛里亚克综合征
Mauriac综合征是1型糖尿病患者血糖控制不良的代谢并发症,儿童特有,其特征为生长衰竭、身材矮小、青春期延迟、库欣样特征,以及糖原大量沉积导致的显著肝肿大。这可能是由于多种因素的综合作用,包括组织中葡萄糖摄取和利用不足,胰岛素样生长因子-1和生长激素水平降低,这些激素的生物活性受损,循环激素抑制剂,激素受体抵抗或缺陷,胰岛素缺乏和血糖控制不良。由于更好的治疗方式,这种综合征现在很少见到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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