Schinzel A
J Med Genet. 1981 Feb;18(1):64-8. doi: 10.1136/jmg.18.1.64.
A mother with a translocation rcp (1;3) (q32;p25) gave birth to a son with duplication of 1q32 leads to qter and deletion of 3p25 leads to pter. At 17 1/2 years of age, the proband was severely mentally retarded and presented a pattern of multiple minor dysmorphic stigmata and anomalies, including hypertrichosis, synophrys, ocular hypertelorism, ptosis, convergent squint, cleft uvula nad narrow palate, poorly modelled auricles, funnel chest, kyphoscoliosis, umbilical and inguinal hernias, and cubitus valgus. He had normal stature and did not have any apparent malformations.
一位患有1;3号染色体相互易位rcp(1;3)(q32;p25)的母亲生下了一个儿子,该儿子存在1号染色体q32至qter重复以及3号染色体p25至pter缺失的情况。先证者在17岁半时严重智力发育迟缓,呈现出多种轻微的畸形体征和异常,包括多毛症、连眉、眼距增宽、上睑下垂、内斜视、悬雍垂裂和腭狭窄、耳廓形态不佳、漏斗胸、脊柱侧凸、脐疝和腹股沟疝以及肘外翻。他身材正常,没有任何明显的畸形。