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米贝利汗孔角化症患者中优先累及3号染色体的克隆性染色体异常。

Clonal chromosome abnormalities with preferential involvement of chromosome 3 in patients with porokeratosis of Mibelli.

作者信息

Scappaticci S, Lambiase S, Orecchia G, Fraccaro M

机构信息

Biologia Generale e Genetica Medica Università di Pavia, Italy.

出版信息

Cancer Genet Cytogenet. 1989 Nov;43(1):89-94. doi: 10.1016/0165-4608(89)90131-3.

Abstract

Clonal chromosome abnormalities were found in cultured fibroblasts from three sibs and one sporadic case with porokeratosis of Mibelli. Chromosome 3 especially involved region p12-14. This region includes the most common fragile site in humans, and the proximal region of chromosome 3 short arm is involved in a variety of neoplastic conditions. We conclude that porokeratosis of Mibelli, an autosomal dominant disorder, is associated with chromosomal instability. Porokeratosis of Mibelli is known to also be associated with increased susceptibility to malignant disease. The chromosome instability may well predispose to malignancy.

摘要

在3例米贝利汗孔角化症患者的同胞以及1例散发患者的培养成纤维细胞中发现了克隆性染色体异常。3号染色体尤其涉及p12 - 14区域。该区域包含人类最常见的脆性位点,并且3号染色体短臂的近端区域涉及多种肿瘤性疾病。我们得出结论,常染色体显性疾病米贝利汗孔角化症与染色体不稳定性相关。已知米贝利汗孔角化症还与恶性疾病易感性增加有关。染色体不稳定性很可能易导致恶性肿瘤。

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