Fryburg J S, Golden W L
Department of Pediatrics, University of Virginia Health Science Center, Charlottesville 22908.
Am J Med Genet. 1993 Mar 1;45(5):638-41. doi: 10.1002/ajmg.1320450524.
We report on a 3-year-old girl who has an interstitial deletion of chromosome 8q [46,XX,del(8)(q13.3q22.1)]. She has severe mental retardation and minor anomalies in addition to lambdoidal synostosis. This is the first report of craniosynostosis in association with this chromosomal deletion. The manifestations of our patient are compared to those of previously reported patients with similar deletions.
我们报告了一名3岁女孩,她存在8号染色体q臂的间质缺失[46,XX,del(8)(q13.3q22.1)]。除人字缝早闭外,她还患有严重智力发育迟缓及轻微异常。这是首例与该染色体缺失相关的颅缝早闭报告。我们将该患者的表现与先前报道的具有类似缺失的患者表现进行了比较。