Eich G F, Silver M M, Weksberg R, Daneman A, Costa T
Department of Radiology, Hospital for Sick Children, University of Toronto.
Radiology. 1991 Oct;181(1):183-8. doi: 10.1148/radiology.181.1.1909446.
Radiographic, clinical, and histologic findings in two infants and a neonate with a syndrome of profoundly accelerated skeletal maturation included features closely resembling those of Marshall-Smith (MS) syndrome, but patients had dysmorphic ears as well as distinctive generalized skeletal abnormalities suggestive of a bone dysplasia. Among these was an instability at the craniocervical junction with severe spinal stenosis. These previously unrecognized abnormalities may represent uncommon manifestations within the spectrum of MS syndrome or indicate the existence of a separate disorder.
两名婴儿和一名新生儿患有骨骼成熟显著加速综合征,其影像学、临床和组织学检查结果包括与马歇尔 - 史密斯(MS)综合征极为相似的特征,但患者有耳部畸形以及提示骨发育异常的独特全身性骨骼异常。其中包括颅颈交界处不稳定伴严重椎管狭窄。这些先前未被认识到的异常可能代表MS综合征范围内不常见的表现,或者表明存在一种单独的疾病。