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唐氏综合征与克兰费尔特综合征的双非整倍体

Double aneuploidy with Down's-Klinefelter's syndrome.

作者信息

Hou J W, Wang T R

机构信息

Department of Pediatrics, National Taiwan University Hospital, Taipei, ROC.

出版信息

J Formos Med Assoc. 1996 Apr;95(4):350-2.

PMID:8935309
Abstract

The occurrence of double aneuploidy, ie, the existence of two chromosomal abnormalities in the same individual, is a relatively rare phenomenon. A 1-year-old boy with Down's syndrome resulting from de novo mosaic 21 trisomy with an additional X in the karyotype: 47,XXY/48,XXY,+21 (4%/96%) is reported. Besides the typical features of Down's syndrome, the patient did not have the commonly associated conditions (recurrent respiratory tract infections, congenital heart disease, thyroid or digestive tract problems). A molecular cytogenetic method with biotin-labeled probe D13Z1/D21Z1 was used to confirm the diagnosis and to clarify the status of Down's syndrome mosaicism which explained the milder stigmata of Down's syndrome in this case. The coexistence of Klinefelter's syndrome (47,XXY) also may have contributed to the development of normal height and micropenis in this patient. To our knowledge, this is the first case of Down's syndrome together with Klinefelter's syndrome in Taiwan.

摘要

双非整倍体的出现,即同一个体存在两种染色体异常,是一种相对罕见的现象。本文报告了一名1岁男孩,其唐氏综合征源于新发的嵌合型21三体,核型为47,XXY/48,XXY,+21(4%/96%),还有一条额外的X染色体。除了唐氏综合征的典型特征外,该患者没有常见的相关病症(反复呼吸道感染、先天性心脏病、甲状腺或消化道问题)。采用生物素标记探针D13Z1/D21Z1的分子细胞遗传学方法来确诊并阐明唐氏综合征嵌合体的状况,这解释了该病例中唐氏综合征症状较轻的原因。克氏综合征(47,XXY)的共存也可能促成了该患者身高正常和小阴茎的发育。据我们所知,这是台湾首例唐氏综合征合并克氏综合征的病例。

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