Tibial agenesis, femoral duplication, and caudal midline anomalies

被引:0
|
作者
Evans, JA
Chudley, AE
机构
[1] Univ Manitoba, Dept Human Genet, Winnipeg, MB R3E 0W3, Canada
[2] Univ Manitoba, Dept Pediat & Child Hlth, Winnipeg, MB R3E 0W3, Canada
[3] Childrens Hosp, Winnipeg, MB R3A 1S1, Canada
[4] Univ Manitoba, Dept Community Hlth Sci, Winnipeg, MB R3T 2N2, Canada
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1999年 / 85卷 / 01期
关键词
tibia; femur; cloaca; bifurcation; duplication; abdominal wall; OEIS; exstrophy; HOX genes; Gollop-Wolfgang;
D O I
10.1002/(SICI)1096-8628(19990702)85:1<13::AID-AJMG5>3.0.CO;2-N
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Tibial agenesis with femoral duplication (Gollop-Wolfgang complex) and cloacal exstrophy are each rare malformations. Thus, their concurrence in an individual is an extremely rare event. We report on a patient born with distal duplication of the right femur, agenesis of the right tibia and hallux, cloacal exstrophy, and sacral defects. Review of the small group of cases reported with femoral duplication and tibial agenesis in association with caudal midline defects demonstrated a pattern of anomalies that while varying in presentation and severity was quite specific. We postulate that this disorder is related to misexpression of one or more distal HOX genes, potentially HOX10 or HOX11, leading to abnormal induction and proliferation of caudal mesenchyme, Am. J, Med. Genet. 85:13-19, 1999, (C) 1999 Wiley-Liss, Inc.
引用
收藏
页码:13 / 19
页数:7
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