骨折的实际原因的情况下,患者随访成骨不全:戈歇病。

Q3 Medicine Clinical Cases in Mineral and Bone Metabolism Pub Date : 2017-09-01 Epub Date: 2017-12-27 DOI:10.11138/ccmbm/2017.14.3.336
Ufuk Demirci, Ahmet Çizmecioglu, Ismet Aydogdu
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引用次数: 1

摘要

戈谢病(GD)是一种罕见的疾病,其特征是网状内皮系统中β-葡萄糖脑苷积累。患者可能以骨痛、肝脾肿大、贫血、血小板减少、生长迟缓、间质性肺疾病、肺动脉高压和骨骼疾病等主诉就诊。骨骼系统受累是常见的戈谢病患者和发病率的重要原因。我们的病人作为一个玻璃儿童被随访了几年-成骨不全,他有关节畸形由于骨骼骨折。我们想提出这个病例,以提高对GD的骨骼累及和晚期诊断的影响的认识。
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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Actual reason for bone fractures in the case of a patient followed-up with the osteogenesis imperfecta: Gaucher's Disease.

Gaucher's disease (GD) is a rare disease characterized by a β-glucocerebroside accumulation in the reticulo-endothelial system. Patients may refer to the clinic with complaints of bone pain, hepatosplenomegaly, anemia, thrombocytopenia, growth retardation, interstitial pulmonary disease, pulmonary hypertension, and skeletal disorders. Skeletal system involvement is observed commonly in Gaucher patients and a significant cause of morbidity. Our patient was followed for several years as a glass child - osteogenesis imperfecta and he had joint deformities due to skeletal fractures. We wanted to present this case to raise awareness of GD's skeletal involvement and effects of late diagnosis.

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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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