Borenstein Z C, Mink J, Oppenheim W, Rimoin D L, Lachman R S
UCLA School of Medicine, Ahmanson Pediatric Center.
Skeletal Radiol. 1991;20(2):134-6. doi: 10.1007/BF00193828.
We describe a patient with the rare autosomal dominant syndrome of congenital glenoid dysplasia. The severity of the findings resulted in an intense and effective radiological and clinical work-up including MRI, CT reconstruction, and fluoroscopy.
我们描述了一位患有罕见的先天性肩胛盂发育不良常染色体显性综合征的患者。检查结果的严重性促使我们进行了全面且有效的影像学和临床检查,包括核磁共振成像(MRI)、CT重建以及荧光透视检查。