Bamforth J S, Kaurah P, Byrne J, Ferreira P
Department of Pediatrics, University of Alberta, Edmonton, Canada.
Am J Med Genet. 1994 Feb 15;49(4):393-6. doi: 10.1002/ajmg.1320490408.
We describe a mother and her 3 children with variable scalp defects and limb defects consistent with a diagnosis of Adams Oliver syndrome also presenting with additional anomalies including congenital heart disease, microcephaly, epilepsy, mental retardation, arrhinencephaly, hydrocephaly, anatomic bronchial anomalies, and renal anomalies. The clinical variation between the individuals is more pronounced than in previously reported families.
我们描述了一位母亲及其3个孩子,他们患有与亚当斯-奥利弗综合征诊断相符的头皮缺损和肢体缺损,还伴有其他异常情况,包括先天性心脏病、小头畸形、癫痫、智力迟钝、无脑回畸形、脑积水、解剖学支气管异常和肾脏异常。个体之间的临床差异比先前报道的家族更为明显。