Ramer J C, Frankel C A, Ladda R L
Department of Pediatrics, Pennsylvania State University College of Medicine, Milton S. Hershey Medical Center, Hershey 17033.
Am J Med Genet. 1993 Feb 1;45(3):285-91. doi: 10.1002/ajmg.1320450302.
The physical, radiographic, and pathologic findings in 3 new patients with Marden-Walker syndrome (MWS) are compared with those of previously described children with the syndrome. Over 75% of the children with MWS have blepharophimosis, psychomotor retardation, small mouth, micrognathia, kyphosis/scoliosis, and multiple contractures. Minimal diagnostic criteria have yet to be defined attesting to the broad range of variability and potential genetic heterogeneity in this disorder.
将3例新诊断的马登-沃克综合征(MWS)患者的体格检查、影像学检查及病理检查结果与之前报道的该综合征患儿进行比较。超过75%的MWS患儿有睑裂狭小、精神运动发育迟缓、小嘴、小颌、脊柱后凸/脊柱侧凸及多处挛缩。由于该疾病存在广泛的变异性及潜在的基因异质性,目前尚未确定其最低诊断标准。