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首例间质性20q11.22-q12微缺失及分子细胞遗传学特征报告病例中的主要喂养困难。

Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization.

作者信息

Callier P, Faivre L, Marle N, Thauvin-Robinet C, Sanlaville D, Gosset P, Prieur M, Labenne M, Huet F, Mugneret F

机构信息

Département de Génétique, CHU Le Bocage, Dijon, France.

出版信息

Am J Med Genet A. 2006 Sep 1;140A(17):1859-63. doi: 10.1002/ajmg.a.31395.

Abstract

We report on a 4-year-old female presenting with intrauterine growth retardation, facial dysmorphic features, major feeding difficulties with severe diarrhea and vomiting, mental retardation with abnormal behavior and hypertonia. Feeding difficulties were the most invalidating features with absent oral intake requiring persistent enteral feeding. Standard cytogenetic studies were normal, but high-resolution chromosome analyses revealed a small de novo interstitial deletion of the long arm of chromosome 20, 46,XX,del(20)(q11.21q12). The deletion was confirmed using metaphase comparative genomic hybridization (CGH) and multicolor high resolution banding (mBAND). The deletion breakpoints were characterized using FISH analyses with YACs, PACs, and BACs clones located in the deleted and adjacent regions. A 6.6-Mb deleted region between markers D20S815 (20q11.22) and D20S435 (20q12) could be delineated. None of the nine previously reported cases with interstitial 20q deletion found in the literature involve the same breakpoints. This report further emphasizes the indication of high-resolution chromosome analyses in children with syndromic mental retardation. The description of additional cases would be useful in order to better characterize the phenotype of patients with proximal interstitial 20q deletion.

摘要

我们报告了一名4岁女性患者,其表现为宫内生长迟缓、面部畸形特征、伴有严重腹泻和呕吐的主要喂养困难、伴有异常行为和张力亢进的智力发育迟缓。喂养困难是最严重的问题,无法经口进食,需要持续肠内喂养。标准细胞遗传学研究结果正常,但高分辨率染色体分析显示20号染色体长臂存在一个小的新发间质性缺失,核型为46,XX,del(20)(q11.21q12)。使用中期比较基因组杂交(CGH)和多色高分辨率显带(mBAND)证实了该缺失。使用位于缺失区域和相邻区域的酵母人工染色体(YAC)、细菌人工染色体(BAC)和噬菌体人工染色体(PAC)克隆进行荧光原位杂交(FISH)分析,对缺失断点进行了特征描述。在标记D20S815(20q11.22)和D20S435(20q12)之间可划定一个6.6Mb的缺失区域。文献中先前报道的9例20号染色体间质性缺失病例均未涉及相同的断点。本报告进一步强调了对患有综合征性智力发育迟缓儿童进行高分辨率染色体分析的必要性。描述更多病例将有助于更好地明确近端20号染色体间质性缺失患者的表型。

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