Sorge G, Ruggieri M, Lachman R S
Clinica Pediatrica, Università di Catania, Italy.
Am J Med Genet. 1995 Nov 6;59(2):139-42. doi: 10.1002/ajmg.1320590204.
We present a patient with spondyloperipheral dysplasia, a rare skeletal dysplasia which is characterized by vertebral body abnormalities (platyspondyly, end-plate indentations) and brachydactyly. Our patient also manifested a characteristic "pugilistic" face, sensorineural deafness and mental retardation. This chondroosseous dysplasia appears to be inherited as an autosomal dominant disorder. It appears that there is considerable clinical variability in spondyloperipheral dysplasia.
我们报告了一名患有脊椎周围发育异常的患者,这是一种罕见的骨骼发育异常疾病,其特征为椎体异常(扁平椎体、终板凹陷)和短指畸形。我们的患者还表现出典型的“拳击手样”面容、感音神经性耳聋和智力发育迟缓。这种软骨骨发育异常似乎是作为常染色体显性疾病遗传的。脊椎周围发育异常似乎存在相当大的临床变异性。