Prune Belly Syndrome Associated with Interstitial 17q12 Microdeletion.

Case Reports in Urology Pub Date : 2022-02-14 eCollection Date: 2022-01-01 DOI:10.1155/2022/7364286
Surasak Puvabanditsin, Miry Shim, Jeffrey Suell, Jeffrey Manzano, Kristin Blackledge, Avram Bursky-Tammam, Rajeev Mehta
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Abstract

We report a term male neonate presenting with a "prune belly," bilateral hydronephrosis, hydroureter, posterior urethral obstruction, and bilateral undescended testes. Analysis with the whole genome SNP microarray revealed an interstitial deletion of about 1.49 megabase (MB) at chromosome 17q12. We present a rare association of prune belly syndrome with a chromosomal deletion in this same region.

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西梅肚综合征与间质17q12微缺失相关。
我们报告一个男性新生儿表现为“梅子肚”,双侧肾积水,输尿管积水,后尿道梗阻和双侧睾丸隐睾。全基因组SNP芯片分析显示,17q12染色体间质缺失约1.49兆碱基(MB)。我们提出了一个罕见的关联梅干腹综合征与染色体缺失在同一区域。
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来源期刊
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发文量
28
审稿时长
13 weeks
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