Suppr超能文献

ROHHAD 综合征——儿童肥胖的一个仍未被认识的病因:三例报告。

ROHHAD syndrome - A still unrecognized cause of childhood obesity: report of three cases.

机构信息

First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, «Aghia Sophia» Children's Hospital, Athens, Greece.

出版信息

J Pediatr Endocrinol Metab. 2020 Sep 30;33(10):1341-1348. doi: 10.1515/jpem-2020-0111.

Abstract

Objectives Rapid-onset obesity with hypoventilation, hypothalamic dysfunction, and autonomic dysregulation (ROHHAD) is a rare, potentially fatal, pediatric syndrome. Case presentations We describe three cases of ROHHAD-syndrome in Greece. The main and earliest symptom was the excessive and rapid weight gain at 5, 2, and 3 years of age. Years after the onset of obesity, the patients developed hypothalamic dysfunction with various endocrinological abnormalities (at 9, 8, and 6.8 years, respectively), autonomic dysregulation and finally, alveolar hypoventilation (at 14.6, 8, and 7.8 years, respectively), leading to the diagnosis of ROHHAD-syndrome. Conclusions The rarity of the syndrome, the variable symptoms' presentation, and the lack of specific diagnostic tests could explain why no previous cases have been reported from our country. The rapid onset of obesity was underestimated, and the patients were misdiagnosed with other more common obesity syndromes. Therefore, we propose a questionnaire to help physicians identify patients with ROHHAD-syndrome.

摘要

目的

快速进展性肥胖伴通气不足、下丘脑功能障碍和自主神经功能紊乱(ROHHAD)是一种罕见的、潜在致命的儿科综合征。

病例介绍

我们在希腊描述了三例 ROHHAD 综合征病例。主要和最早的症状是 5 岁、2 岁和 3 岁时体重过度快速增加。肥胖发生多年后,患者出现下丘脑功能障碍和各种内分泌异常(分别为 9 岁、8 岁和 6.8 岁)、自主神经功能紊乱,最终出现肺泡通气不足(分别为 14.6 岁、8 岁和 7.8 岁),从而诊断为 ROHHAD 综合征。

结论

该综合征罕见,症状表现多样,缺乏特异性诊断试验,这可能解释了为何在我国以前没有报告过该病例。肥胖的快速发作被低估了,患者被误诊为其他更常见的肥胖综合征。因此,我们提出了一个问卷,以帮助医生识别 ROHHAD 综合征患者。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验