部分三体性
三体
单体
精神运动迟缓
儿科
医学
遗传学
心理学
生物
病理
核型
染色体
基因
替代医学
作者
Jennifer A. Roggenbuck,James M. Fink,Nancy J. Mendelsohn
出处
期刊:American journal of medical genetics
[Wiley]
日期:2001-01-01
卷期号:101 (1): 50-54
被引量:17
摘要
We report a 3-year-old girl with trisomy 2p24.3-pter who presented with marked psychomotor delay and dysmorphic features. This patient represents the only known case of trisomy 2p24.3-2pter that does not involve an associated functional monosomy. In contrast to recent reports highlighting the fatal or serious complications in patients described as having partial trisomy 2p, this patient does not have significant birth defects or life threatening medical problems. Notably, this patient does not have a neural tube defect (NTD), which has been attributed to a putative locus at 2p24 in other patients with a partial trisomy 2p. © 2001 Wiley-Liss, Inc.
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