Addor M C, Stefanutti D, Farron F, Meinecke P, Lacombe D, Sarlangue J, Prescia G, Schorderet D F
Division of Medical Genetics, CHUV, Lausanne, Switzerland.
Genet Couns. 1995;6(2):113-20.
We report on a 6-year-old girl with C-trigonocephaly syndrome and diaphragmatic hernia. She is severely mentally retarded and shows the characteristic findings of this syndrome, including trigonocephaly, unusual facial features, especially intra-oral anomalies, low set and dysplastic ears, cardiac anomaly and neonatal hypotonia. Following our presentation at the 5th European meeting of dysmorphology in Strasbourg, P. Meinecke brought to our attention a case of C-trigonocephaly who died in the neonatal period from complications of a diaphragmatic hernia. Another case of C-trigonocephaly without diaphragmatic hernia was communicated to us by D. Lacombe. We report these three observations and present a review of 26 alleged cases.
我们报告了一名患有C型三角头畸形综合征和膈疝的6岁女孩。她严重智力发育迟缓,并表现出该综合征的典型特征,包括三角头畸形、特殊的面部特征,尤其是口腔内异常、低位且发育不良的耳朵、心脏异常和新生儿肌张力减退。在我们于斯特拉斯堡举行的第五届欧洲畸形学会议上发表报告后,P. 迈内克让我们注意到一例C型三角头畸形患儿,该患儿在新生儿期因膈疝并发症死亡。D. 拉孔布向我们通报了另一例无膈疝的C型三角头畸形病例。我们报告这三例观察结果,并对26例疑似病例进行综述。