严重智力迟钝和幼年特发性关节炎患者两种独立核型异常的分子细胞遗传学特征。

IF 3.5 Q1 EDUCATION & EDUCATIONAL RESEARCH Genomic medicine Pub Date : 2007-01-01 Epub Date: 2007-07-11 DOI:10.1007/s11568-007-9008-3
Sabine Leybrand, Eva Rossier, Gotthold Barbi, David N Cooper, Hildegard Kehrer-Sawatzki
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引用次数: 0

摘要

我们报告一个患者严重的智力低下,畸形的特点,以及青少年特发性关节炎。g带显示该患者有两种独立的核型异常:间质缺失(X)(p21p22.3)和1号和7号染色体重排,代表直接插入,ins(7;1)(q36;p13.2p31.2)。在血液淋巴细胞和成纤维细胞中观察到父源性del(X)染色体的非随机失活。随后,对1号和7号染色体重排的高分辨率分析显示,在1p13.2断点处,额外的亚显微镜下缺失了至少5mb。缺失发生在父系染色体上,包含PTPN22基因,已知与幼年特发性关节炎有关。我们的研究结果强调了密切研究异常表型患者中明显平衡重排的断点区域的重要性,因为复杂染色体重排(CCRs)可能是不平衡的。
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Molecular cytogenetic characterization of two independent karyotypic anomalies in a patient with severe mental retardation and juvenile idiopathic arthritis.

We report on a patient with severe mental retardation, dysmorphic features as well as juvenile idiopathic arthritis. G-banding indicated two independent karyotypic anomalies in this patient: an interstitial deletion del(X)(p21p22.3) and a rearrangement involving chromosomes 1 and 7, which represents a direct insertion, ins(7;1)(q36;p13.2p31.2). Non-random inactivation of the paternally derived del(X) chromosome was observed in blood lymphocytes and fibroblasts. High resolution analysis of the rearrangement involving chromosomes 1 and 7 subsequently revealed the additional submicroscopic deletion of at least 5 Mb at the 1p13.2 breakpoint. The deletion occurred on the paternal chromosome and encompasses the PTPN22 gene, already known to be associated with juvenile idiopathic arthritis. Our findings underline the importance of closely investigating the breakpoint regions of apparently balanced rearrangements in patients with abnormal phenotypes since complex chromosomal rearrangements (CCRs) may turn out to be unbalanced.

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