Schrander-Stumpel C, de Die-Smulders C, de Krom M, Schyns-Fleuran S, Hamel B, Jaeken D, Fryns J P
Department of Clinical Genetics, Maastricht University Hospital, The Netherlands.
Clin Genet. 1993 Jun;43(6):303-8. doi: 10.1111/j.1399-0004.1993.tb03823.x.
The Marden-Walker syndrome is characterized by psychomotor retardation, a mask-like face with blepharophimosis, micrognathia and a high-arched or cleft palate, low-set ears, kyphoscoliosis and joint contractures. We report on a male patient with the clinical features of the syndrome. In addition, he had a Dandy-Walker malformation with hydrocephalus and vertebral abnormalities. During pregnancy, there were feeble fetal movements and polyhydramnios. We propose that Marden-Walker syndrome is one of the etiologic possibilities in children with the heterogeneous fetal a(hypo)kinesia deformation sequence (FADS). Differential diagnosis is discussed. The etiology is probably heterogeneous.
马登-沃克综合征的特征为精神运动发育迟缓、睑裂狭小的面具样面容、小颌、高拱腭或腭裂、低位耳、脊柱侧凸和关节挛缩。我们报告了一名具有该综合征临床特征的男性患者。此外,他还患有丹迪-沃克畸形伴脑积水和椎体异常。孕期胎动微弱且羊水过多。我们认为马登-沃克综合征是胎儿运动减少(或)变形序列(FADS)异质性患儿的病因之一。文中讨论了鉴别诊断。病因可能具有异质性。