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首页> 外文期刊>Orphanet journal of rare diseases >Obesity in achondroplasia patients: from evidence to medical monitoring
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Obesity in achondroplasia patients: from evidence to medical monitoring

机译:软骨发育不全患者的肥胖:从证据到医学监测

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Abstract Achondroplasia is a rare genetic disease representing the most common form of short-limb dwarfism. It is characterized by bone growth abnormalities that are well characterized and by a strong predisposition to abdominal obesity for which causes are unknown. Despite having aroused interest at the end of the 20?h century, there are still only very little data available on this aspect of the pathology. Today, interest is rising again, and some studies are now proposing mechanistic hypotheses and guidance for patient management. These data confirm that obesity is a major health problem in achondroplasia necessitating an early yet complex clinical management. Anticipatory care should be directed at identifying children who are at high risk to develop obesity and intervening to prevent the metabolic complications in adults. In this review, we are regrouping available data characterizing obesity in achondroplasia and we are identifying the current tools used to monitor obesity in these patients.
机译:摘要软骨病是一种罕见的遗传疾病,代表了短肢侏儒症的最常见形式。它的特征是骨骼生长异常,特征明确,对腹部肥胖的诱因很强,原因不明。尽管在20世纪末期引起了人们的兴趣,但关于病理学这方面的数据仍然很少。如今,人们的兴趣再次上升,并且一些研究现在提出了机械假说和对患者管理的指导。这些数据证实,肥胖是软骨发育不全的主要健康问题,需要早期而复杂的临床处理。预期护理应针对识别有肥胖风险的高危儿童并进行干预以预防成人的代谢并发症。在这篇综述中,我们将重新整理表征软骨发育不良的肥胖症的可用数据,并确定用于监测这些患者肥胖症的当前工具。

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