van Bon Bregje W M, Koolen David A, Feenstra Ilse, Neefs Ineke, Pfundt Rolph, Smeets Dominique F, de Vries Bert B A
Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Clin Dysmorphol. 2007 Oct;16(4):279-82. doi: 10.1097/MCD.0b013e3282630818.
We present a 4-year-old boy with developmental delay and several into minor dysmorphic features due to an interstitial deletion of 17.5 Mb on the long arm of chromosome 13 [46,XY,del (13)(q14.3q21.33)]. The deletion was detected initially during routine cytogenetic screening and further analyzed on a genome-wide BAC array. In contrast to several previous papers reporting a short stature, our patient was tall with a 1 year advanced skeletal age. In this paper, we compare growth and clinical features of this patient with previously reported cases, with a similar interstitial deletion on the long arm of chromosome 13.
我们报告一名4岁男孩,因13号染色体长臂存在17.5 Mb的间质性缺失[46,XY,del(13)(q14.3q21.33)],出现发育迟缓及一些轻微的畸形特征。该缺失最初在常规细胞遗传学筛查中被检测到,并在全基因组BAC阵列上进行了进一步分析。与之前几篇报道身材矮小的论文不同,我们的患者身材高大,骨骼年龄超前1岁。在本文中,我们将该患者的生长和临床特征与之前报道的、13号染色体长臂存在类似间质性缺失的病例进行了比较。