成人低磷酸酶血症的临床表现和疾病负担。

Q3 Medicine Clinical Cases in Mineral and Bone Metabolism Pub Date : 2017-05-01 Epub Date: 2017-10-25 DOI:10.11138/ccmbm/2017.14.1.230
Francesco Conti, Lorenzo Ciullini, Giuseppe Pugliese
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引用次数: 41

摘要

磷酸酶减退症(HPP)是一种罕见的遗传性疾病,其临床表现具有异质性。成人形式的HPP往往难以识别,诊断延误和治疗不当。虽然HPP的严重程度随着发病年龄的增长而降低,但重要的并发症可能发生在任何年龄,成人患者的HPP负担显著。成年HPP患者患有慢性疼痛、复发性骨折和其他骨科问题,并伴有严重的残疾,对他们生活的各个方面都产生了严重的负面影响。本文的目的是总结成人HPP患者的主要方面,回顾文献,并重点介绍患有这种疾病的患者的负担。
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Hypophosphatasia: clinical manifestation and burden of disease in adult patients.

Hypophosphatasia (HPP) is a rare inherited disease with a heterogeneous clinical expression. The adult form of HPP is often difficult to be recognized with a delayed diagnosis and inappropriate treatments. Though severity of HPP decreases with age at onset, important complications could occur at any age and the burden of HPP among adult patients is found to be significant. Adult patients with HPP suffer of chronic pain, recurrent fractures and other orthopedics problems, with severe disability that have a serious negative impact on all aspects of their life. The aim of this paper is to summarize the main aspects of HPP in adult patients reviewing the literature and focusing on its burden for patients suffering from this condition.

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来源期刊
Clinical Cases in Mineral and Bone Metabolism
Clinical Cases in Mineral and Bone Metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
2.60
自引率
0.00%
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0
期刊介绍: The Journal encourages the submission of case reports and clinical vignettes that provide new and exciting insights into the pathophysiology and characteristics of disorders related to skeletal function and mineral metabolism and/or highlight pratical diagnostic and /or therapeutic considerations.
期刊最新文献
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