Loomer R L
Department of Orthopedics, University of British Columbia, Canada.
Clin Orthop Relat Res. 1989 Jan(238):112-6.
Hereditary oncycho-osteodysplasia is a well-defined clinical entity consisting of four characteristics: (1) complete or partial absence of finger and thumb nails typically more severe on the radial side of the hand; (2) bony dysplasia about the knee consisting of patellar and lateral femoral condylar hypoplasia; (3) bony dysplasia about the elbow consisting of hypoplasia of the capitellum and radial head; and (4) iliac horns. The hereditary pattern is autosomal dominant with complete penetrance and variable expressivity. Other associated dysplasias have been reported, but there are only six articles reporting shoulder dysplasia and some of these are of questionable validity. This article reports the clinical and roentgenographic findings of a patient with an obvious deformity of the scapula consisting of a small acromion in both the anteroposterior (AP) and lateral planes. The acromion was deformed and slanted upwards at the lateral border. A slightly attenuated glenoid pointed laterally or slightly inferiorly, giving a humeral acromial interval of 2.5 cm.
遗传性甲-骨发育异常是一种明确的临床病症,具有以下四个特征:(1)手指和拇指甲完全或部分缺失,通常在手部桡侧更为严重;(2)膝关节周围的骨发育异常,包括髌骨和股骨外侧髁发育不全;(3)肘关节周围的骨发育异常,包括肱骨小头和桡骨头发育不全;(4)髂角。遗传模式为常染色体显性遗传,具有完全外显率和可变表达性。其他相关的发育异常也有报道,但仅有六篇文章报道了肩胛骨发育异常,其中一些文章的有效性存疑。本文报告了一名患者的临床和X线表现,该患者肩胛骨明显畸形,在前后位(AP)和侧位平面上均表现为肩峰小。肩峰变形,外侧缘向上倾斜。肩胛盂略变细,指向外侧或略向下,肱肩间隙为2.5厘米。