Osterberg P H, Wallace R G, Adams D A, Crone R S, Dickson G R, Kanis J A, Mollan R A, Nevin N C, Sloan J, Toner P G
Royal Victoria Hospital, Belfast, Northern Ireland.
J Bone Joint Surg Br. 1988 Mar;70(2):255-60. doi: 10.1302/0301-620X.70B2.3346299.
We report 40 cases in one family of an autosomal dominant bone dysplasia, which, though similar in some aspects to Paget's disease, seems unique in some features and in its natural history. The disease shows both general and focal skeletal changes, the latter being mainly in the limbs with an onset from the second decade. Progressive osteoclastic resorption is accompanied by medullary expansion which leads to pain, severe deformity and a tendency to pathological fracture. The serum alkaline phosphatase and urinary hydroxyproline are variably elevated, while other biochemical indices are normal. Most patients had an associated deafness of early onset and loss of dentition. No previous description of this disease has been found in the literature.
我们报告了一个常染色体显性骨发育不良家族中的40个病例。该疾病虽然在某些方面与佩吉特氏病相似,但在某些特征及其自然病史方面似乎具有独特性。这种疾病表现出全身性和局灶性骨骼变化,后者主要发生在四肢,发病始于第二个十年。进行性破骨细胞吸收伴有骨髓扩张,导致疼痛、严重畸形和病理性骨折倾向。血清碱性磷酸酶和尿羟脯氨酸有不同程度升高,而其他生化指标正常。大多数患者伴有早发性耳聋和牙列缺失。文献中未发现此前对该疾病的描述。