Engelbert R H, Gerver W J, Breslau-Siderius L J, van der Graaf Y, Pruijs H E, van Doorne J M, Beemer F A, Helders P J
Department of Pediatric Physical Therapy, University Hospital for Children and Youth, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
Acta Orthop Scand. 1998 Jun;69(3):283-6. doi: 10.3109/17453679809000931.
We examined in a cross-sectional study, 47 children (mean age 7.7 (1-16) years) with osteogenesis imperfecta (OI) to find the prevalence of spinal deformities and to correlate these observations with anthropometry. The associations between dentinogenesis imperfecta, joint hypermobility and spinal deformities were also studied. Disproportion in stature in OI type I and type IV was mainly caused by spinal involvement, as evidenced by a greater decrease in body height than in leg length. In OI type I, the decrease in sitting height was mainly caused by platyspondyly, whereas in OI types III and IV, it was also caused by progressive scoliosis and kyphosis. Scoliosis was present in 22 children, and pathological kyphosis in 18, mainly in the severe OI types. Basilar impression was observed in 10 children, mainly in type III. Children with dentinogenesis imperfecta seemed to be prone to develop scoliosis, pathological kyphosis and basilar impression. Children with generalized joint hypermobility were less prone to develop scoliosis and basilar impression. Our observations may contribute to a better understanding of the risk factors for progressive spinal deformities in OI.
在一项横断面研究中,我们检查了47例成骨不全(OI)患儿(平均年龄7.7(1 - 16)岁),以确定脊柱畸形的患病率,并将这些观察结果与人体测量学相关联。我们还研究了牙本质生成不全、关节活动过度与脊柱畸形之间的关联。I型和IV型OI患儿的身材比例失调主要由脊柱受累引起,身高下降幅度大于腿长下降幅度即证明了这一点。在I型OI中,坐高下降主要由扁平椎体引起,而在III型和IV型OI中,坐高下降还由进行性脊柱侧凸和后凸引起。22例患儿存在脊柱侧凸,18例存在病理性后凸,主要见于严重的OI类型。10例患儿观察到颅底凹陷,主要见于III型。牙本质生成不全的患儿似乎更容易发生脊柱侧凸、病理性后凸和颅底凹陷。全身关节活动过度的患儿发生脊柱侧凸和颅底凹陷的可能性较小。我们的观察结果可能有助于更好地理解OI患儿进行性脊柱畸形的危险因素。