Jasiewicz Barbara, Kacki Wojciech
Department of Orthopedics and Rehabilitation, Jagiellonian University Collegium Medicum, Balzera 15, 34-500 Zakopane, Poland.
Children (Basel). 2023 Mar 19;10(3):589. doi: 10.3390/children10030589.
Abnormalities in cellular differentiation during embryo-fetal period may lead to various malformations of the spine. Caudal regression syndrome (CRS) is a group of defects with premature growth/development termination of the vertebral column. CRS can be divided into three types: sirenomelia, complete absence of the sacrum and partial absence of the sacrum. Genitourinary and gastrointestinal anomalies are common, with neurogenic bladder and bowel incontinence. Treatment of patients with CRS is complex and multidisciplinary and should be comprehensive. The most common orthopedic problems are: spinal deformity (kyphosis and scoliosis), spinopelvic instability and lower limbs deformities.
胚胎-胎儿期细胞分化异常可能导致脊柱的各种畸形。尾椎退化综合征(CRS)是一组因脊柱过早停止生长/发育而出现的缺陷。CRS可分为三种类型:美人鱼综合征、骶骨完全缺失和骶骨部分缺失。泌尿生殖系统和胃肠道异常很常见,伴有神经源性膀胱和肠道失禁。CRS患者的治疗复杂且需要多学科参与,应全面进行。最常见的骨科问题有:脊柱畸形(后凸和脊柱侧凸)、脊柱骨盆不稳定和下肢畸形。