Saul R A, Rogers R C, Phelan M C, Stevenson R E
Greenwood Genetic Center, SC 29646.
Am J Med Genet. 1993 Nov 15;47(7):999-1002. doi: 10.1002/ajmg.1320470712.
We describe 4 patients with facial changes of Brachmann-de Lange syndrome but without limb defects. Mental retardation ranged from moderate to severe and the degree of prenatal and postnatal growth deficiency was variable. These patients exemplify the diagnostic difficulties and counseling dilemmas posed by the mild Branchmann-de Lange phenotype. The relationship of the mild phenotype to the full syndrome will not be understood until the pathogenetic or causal factor(s) are delineated.
我们描述了4例患有布-德二氏综合征面部改变但无肢体缺陷的患者。智力发育迟缓程度从中度到重度不等,产前和产后生长发育不足的程度也各不相同。这些患者体现了轻度布-德二氏综合征表型所带来的诊断困难和咨询困境。在明确发病机制或致病因素之前,轻度表型与完全综合征之间的关系将无法被理解。