Saleem Sidra, Anwar Arsalan, Iftikhar Pulwasha M, Anjum Zauraiz, Tariq Zemal
Neurology, University of Toledo, Toledo, USA.
Neurology, University Hospitals Cleveland Medical Center, Cleveland, USA.
Cureus. 2019 Jul 8;11(7):e5101. doi: 10.7759/cureus.5101.
Spondyloepiphysal dysplasia (SED) is an inheritable dysplasia of the bone due to a defect in collagen. It has a prevalence of 3.4 per million. It has two important types, congenita and tarda, which are differentiated by the age presentation and heritage mode. SED congenita can present a significant reduction in the upper segment to a lower segment ratio. Collagen mutation results in abnormal growth and development of spine and limb bones. The complex pattern of craniofacial anomalies is due to defective ossification and connective tissue problem. We here present the case of a three-hour-old girl with a short trunk and craniofacial anomalies that brought in respiratory distress to the neonatal intensive care unit. This condition is rare and thus poses a major diagnostic challenge at an early stage.
脊椎骨骺发育不良(SED)是一种由于胶原蛋白缺陷导致的遗传性骨骼发育不良。其发病率为百万分之3.4。它有两种重要类型,即先天性和迟发性,可通过发病年龄和遗传方式进行区分。先天性SED可表现为上身与下身比例显著降低。胶原蛋白突变导致脊柱和四肢骨骼的异常生长和发育。颅面畸形的复杂模式是由于骨化缺陷和结缔组织问题所致。我们在此报告一例3小时大的女婴病例,该女婴躯干短小且有颅面畸形,因呼吸窘迫被送入新生儿重症监护病房。这种情况很罕见,因此在早期阶段构成了重大的诊断挑战。