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Implementing a screening program for acromegaly in Latin America: necessity versus feasibility

机译:在拉丁美洲实施一项针对肢端肥大症的筛查计划:必要性与可行性

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摘要

IntroductionAcromegaly is a rare disease with a large burden due its associated comorbidities and the life-long management required. Since the occurrence and severity of associated complications are related to length of exposure to the excess growth hormone seen in acromegaly, early diagnosis is imperative. The delay in diagnosis, however, can be long, and may be the result of a lack of disease awareness and screening programs. Since acromegaly is an uncommon disease, finding ways to increase recognition and diagnosis that would permit early detection in a logical and cost-effective manner could be a challenge.
机译:简介肢端肥大症是一种罕见的疾病,负担重,归因于其相关的合并症和终生管理。由于相关并发症的发生和严重程度与肢端肥大症中过量生长激素的暴露时间有关,因此必须尽早诊断。但是,诊断的延迟可能会很长,并且可能是由于缺乏疾病意识和筛查程序所致。由于肢端肥大症是一种罕见的疾病,因此寻找能够以合理且具有成本效益的方式进行早期发现的增加识别和诊断的方法可能是一个挑战。

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