Richieri-Costa A, Colletto G M, Gollop T R, Masiero D
Am J Med Genet. 1985 Apr;20(4):631-8. doi: 10.1002/ajmg.1320200409.
We describe two sibs born to a consanguineous couple. Among other clinical findings both have mental retardation, short stature, facial and skeletal abnormalities characterized by hypertelorism, broad notched nasal tip, cleft lip/palate, campto-brachy-poly-syndactyly, fibular hypoplasia, and marked anomalies of foot structures. Facial signs of the reported patients resemble those present in the fronto-nasal "dysplasia" syndrome; however, the whole clinical picture in the present patients suggests a true MCA/MR syndrome, most likely inherited as an autosomal recessive trait. Clinical and genetic aspects of the present family are discussed.
我们描述了一对近亲结婚夫妇所生的两个同胞。在其他临床发现中,两人均有智力发育迟缓、身材矮小、面部和骨骼异常,其特征为眼距过宽、鼻尖宽阔有缺口、唇腭裂、弯臂短指多指畸形、腓骨发育不全以及足部结构明显异常。报告患者的面部体征与额鼻“发育异常”综合征中的体征相似;然而,目前患者的整体临床情况提示为一种真正的小头畸形/智力发育迟缓综合征,很可能作为常染色体隐性性状遗传。本文讨论了该家族的临床和遗传学方面情况。