Department of Pediatric and Adolescent Medicine, Villa Metabolica, University Medical Center of the Johannes Gutenberg, University of Mainz, Langenbeckstrasse 2, Mainz 55131, Germany.
Rheum Dis Clin North Am. 2013 May;39(2):431-55. doi: 10.1016/j.rdc.2013.03.004.
Mucopolysaccharidosis and other lysosomal storage diseases are rare, chronic, and progressive inherited diseases caused by a deficit of lysosomal enzymes. Patients are affected by a wide variety of symptoms. For some lysosomal storage diseases, effective treatments to arrest disease progression, or slow the pathologic process, and increase patient life expectancy are available or being developed. Timely diagnosis is crucial. Rheumatologists, orthopedics, and neurologists are commonly consulted due to unspecific musculoskeletal signs and symptoms. Pain, stiffness, contractures of joints in absence of clinical signs of inflammation, bone pain or abnormalities, osteopenia, osteonecrosis, secondary osteoarthritis or hip dysplasia are the alerting symptoms that should induce suspicion of a lysosomal storage disease.
黏多糖贮积症和其他溶酶体贮积症是由溶酶体酶缺乏引起的罕见、慢性和进行性遗传性疾病。患者受多种症状影响。对于一些溶酶体贮积症,已有或正在开发可阻止疾病进展、减缓病理过程和延长患者预期寿命的有效治疗方法。及时诊断至关重要。由于非特异性肌肉骨骼体征和症状,风湿病医生、骨科医生和神经科医生经常被咨询。无炎症临床体征情况下的关节疼痛、僵硬、挛缩、骨痛或异常、骨质疏松症、骨坏死、继发性骨关节炎或髋关节发育不良是应引起对溶酶体贮积症怀疑的警示症状。