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无虹膜和/或肾母细胞瘤患者的过氧化氢酶水平:效用与局限性

Catalase levels in patients with aniridia and/or Wilms' tumor: utility and limitations.

作者信息

Ferrell R E, Riccardi V M

出版信息

Cytogenet Cell Genet. 1981;31(2):120-3. doi: 10.1159/000131636.

Abstract

The gene for red blood cell (RBC) catalase has recently been mapped to 11p13, and a gene dosage effect has been demonstrated for individuals with triplication or deletion of that region. Deletion of the 11p13 band has also been associated with aniridia, with and without Wilm's tumor. We studied the RBC catalase levels in individuals without detectable chromosomal abnormalities but with aniridia, Wilm's tumor, and the combination of aniridia and Wilms' tumor, to determine whether catalase levels might provide evidence for a submicroscopic chromosomal deletion in the 11p13 region. All karyotypically normal patients were found to have normal catalase levels.

摘要

红细胞(RBC)过氧化氢酶基因最近已被定位到11p13,并且已证明该区域存在三倍体或缺失的个体存在基因剂量效应。11p13带的缺失也与有无威尔姆斯瘤的无虹膜症有关。我们研究了无明显染色体异常但患有无虹膜症、威尔姆斯瘤以及无虹膜症和威尔姆斯瘤合并症的个体的红细胞过氧化氢酶水平,以确定过氧化氢酶水平是否可能为11p13区域的亚显微染色体缺失提供证据。所有核型正常的患者过氧化氢酶水平均正常。

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