Clark C E, Cowell H R, Telfer M A, Casey P A
Am J Med Genet. 1980;5(2):171-8. doi: 10.1002/ajmg.1320050211.
Chromosome banding was used to define a partial duplication of the long arm of chromosome 6 (6q25 leads to 6qter) in two profoundly affected sisters and to identify their phenotypically normal mother and sister as balanced translocation carriers whose karyotypes were interpreted as 46,XX,t(6;11) (q25;q25). Prominent clinical features included profound mental retardation, hypertelorism, micrognathia, down-turned mouth, dental anomalies, clubfeet, webbed neck, late progressive scoliosis, flexion contractures, and low total finger ridge count. By comparison with published reports, it has been possible to establish a trisomy 6q25 leads to 6qter syndrome.
染色体显带技术被用于确定两名严重患病姐妹的6号染色体长臂部分重复(6q25至6qter),并将她们表型正常的母亲和姐妹鉴定为平衡易位携带者,其核型被解释为46,XX,t(6;11)(q25;q25)。突出的临床特征包括严重智力迟钝、眼距过宽、小颌畸形、嘴角下垂、牙齿异常、马蹄内翻足、蹼颈、晚期进行性脊柱侧弯、屈曲挛缩以及手指总嵴纹数低。通过与已发表报告进行比较,得以确定一种6q25至6qter三体综合征。