Kaur Harmeet, Gupta Kamini, Tiwari Punit
Department of Radiodiagnosis, Dayanand Medical College & Hospital, India.
Department of Orthopedics, Government Medical College, India.
SA J Radiol. 2018 Jun 14;22(1):1326. doi: 10.4102/sajr.v22i1.1326. eCollection 2018.
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disorder with predominant membranous bone involvement. It may also occur as a sporadic mutation. The diagnosis of this condition is based on the clinical, radiological and genetic findings. It is characterised by hypoplasia or aplasia of the lateral thirds of the clavicles; craniofacial and dental anomalies; and hypoplastic iliac bones. Pyknodysostosis is a close radiological mimic of this entity. Definite diagnosis is based on the genetic analysis. A 36-year-old short-statured female was referred for computed tomography of the paranasal regions for complaints of a deviated nasal septum and midline depression in her forehead. Skeletal screening demonstrated an open metopic suture, wormian bones, maxillary hypoplasia, maldentition and aplastic lateral thirds of both clavicles. In this article, we report a case of CCD, discuss various overlapping features between CCD and pyknodysostosis and attempt to differentiate them radiologically.
锁骨颅骨发育不全(CCD)是一种罕见的常染色体显性骨骼疾病,主要累及膜性骨。它也可能作为散发性突变出现。这种疾病的诊断基于临床、放射学和遗传学检查结果。其特征为锁骨外侧三分之一发育不全或缺失;颅面及牙齿异常;以及髂骨发育不全。致密性骨发育不全在放射学上与该疾病极为相似。明确诊断基于基因分析。一名36岁身材矮小的女性因鼻中隔偏曲和前额中线凹陷的主诉前来接受鼻旁区域的计算机断层扫描。骨骼筛查显示额缝未闭、缝间骨、上颌骨发育不全、牙列不齐以及双侧锁骨外侧三分之一缺失。在本文中,我们报告一例CCD病例,讨论CCD与致密性骨发育不全之间的各种重叠特征,并尝试从放射学角度对它们进行鉴别。