Parloir C, Fryns J P, Van den Berghe H
Hum Genet. 1979 Apr 5;47(3):239-44. doi: 10.1007/BF00321015.
Two profoundly mentally retarded brothers with partial trisomy for the distal part of the short arm of chromosome 3 (3p25 to 3pter) are described. Their anomaly arose as a segregation product of a balanced t(3p-;18q+) translocation in the mother. Compared with the other cases of partial 3p trisomy reported up to now, the present patients display a similar craniofacial dysmorphism with hypertelorism, broad nasal tip, short upper lip with prominent philtrum, and a large mouth with down-turned corners. Other stigmata, such as a prominent, high forehead with frontal bossing and full cheeks, were present during childhood but progressively disappeared.
本文描述了两名患有3号染色体短臂远端部分(3p25至3pter)部分三体性的重度智力障碍兄弟。他们的异常情况是母亲平衡易位t(3p-;18q+)的分离产物。与迄今为止报道的其他部分3p三体病例相比,这两名患者表现出相似的颅面畸形,包括眼距增宽、鼻尖宽阔、上唇短且人中突出、口角下垂的大嘴。其他体征,如额部突出、前额隆起和脸颊丰满的高额头,在儿童期出现,但逐渐消失。