Bagatelle R, Cassidy S B
Department of Pediatrics, University of Arizona College of Medicine, Tucson, USA.
Am J Med Genet. 1995 Jan 30;55(3):367-71. doi: 10.1002/ajmg.1320550324.
We describe a boy with an apparently unique constellation of anomalies, including macrocephaly, short stature, relatively short limbs, hearing loss, developmental delay, sparse anterior scalp hair, hypertelorism, downslanting palpebral fissures, and a short nose with a broad, flat nasal bridge and anteverted nares. Chromosomes were normal and radiographs failed to show a bone dysplasia. We conclude that this represents a new syndrome.
我们描述了一个患有明显独特异常组合的男孩,包括巨头畸形、身材矮小、四肢相对较短、听力丧失、发育迟缓、前头皮毛发稀疏、眼距过宽、睑裂向下倾斜,以及鼻梁宽平且鼻孔前倾的短鼻。染色体正常,X线片未显示骨发育异常。我们得出结论,这代表一种新的综合征。