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唐氏综合征中的7号染色体长臂等臂染色体

Isochromosome 7q in Down syndrome.

作者信息

Wong K F, Lam S C, Leung Jennifer N S

机构信息

Department of Pathology, Queen Elizabeth Hospital, 30 Gascoigne Road, Kowloon, Hong Kong SAR, China.

出版信息

Cancer Genet Cytogenet. 2006 Jan 15;164(2):152-4. doi: 10.1016/j.cancergencyto.2005.07.014.

Abstract

Isochromosome 7q is not an uncommon chromosomal abnormality. It has been reported in association with Shwachman-Diamond syndrome, Wilms tumor, and hepatosplenic T-cell lymphoma. In other hematolymphoid malignancies, it occurs almost invariably as a secondary change. A notable example is its association with t(4;11)(q21;q23) in acute lymphoblastic leukemia. It has rarely been described in myelodysplastic syndrome and acute myeloid leukemia. We report the occurrence of i(7q) as the primary abnormality in a 2-year-old boy with Down syndrome and minimally differentiated acute myeloid leukemia.

摘要

7号染色体长臂等臂染色体是一种并不罕见的染色体异常。已有报道其与施-戴二氏综合征、肾母细胞瘤和肝脾T细胞淋巴瘤相关。在其他血液淋巴系统恶性肿瘤中,它几乎总是作为继发性改变出现。一个显著的例子是其与急性淋巴细胞白血病中的t(4;11)(q21;q23)相关。在骨髓增生异常综合征和急性髓系白血病中很少有相关描述。我们报告了一名患有唐氏综合征和微分化急性髓系白血病的2岁男孩中出现i(7q)作为主要异常情况。

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