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应用荧光原位杂交技术对一条衍生17号染色体进行特征分析。

Characterization of a derivative chromosome 17 by fish-technique.

作者信息

Ramesh K H, Shah H O, Sherman J, Lin J H, Verma R S

机构信息

Division of Genetics, Long Island College Hospital, SUNY Health Science Center at Brooklyn, USA.

出版信息

Ann Genet. 1996;39(3):177-80.

PMID:8839891
Abstract

We report a case with derivative chromosome 17 which could not be characterized by routine G-banding, since the additional material on 17q overlapped with chromosome bands 2q35 -->qter, 3p25-->pter, 4p15-->pter, 5q33-->qter, 7p15-->pter, 12p11.2-->pter, 14q24-->qter and 16q22-->qter. Therefore, whole chromosome paint and region specific probes were used to identify the abnormality by FISH-technique which revealed a 46,XY, der (17) t (4;17) (p15.2;q25) karyotype. The proband was partially trisomic for 4p15.2-->pter and monosomic for the distal 17q25-->qter regions. The major clinical features included: anti-mongoloid slanted palpebrae, coloboma of right iris, depressed nasal bridge, high arched palate, protruding tongue, micrognathia and small penis. The MRI of the brain revealed midly hypoplastic cerebellar vermis, and a normal septum pellucidum. The infant responded to therapy for hypoglycemia and was discharged under stable condition. Prior to cytogenetic evaluation the infant was not recognized as either "trisomy 4p syndrome" or "monosomy 17q syndrome".

摘要

我们报告了一例17号衍生染色体病例,由于17q上的额外物质与2q35→qter、3p25→pter、4p15→pter、5q33→qter、7p15→pter、12p11.2→pter、14q24→qter和16q22→qter染色体带重叠,常规G显带无法对其进行特征描述。因此,使用全染色体涂染探针和区域特异性探针通过荧光原位杂交(FISH)技术来鉴定异常,结果显示核型为46,XY, der(17)t(4;17)(p15.2;q25)。先证者4p15.2→pter区域部分三体,17q25→qter远端区域单体。主要临床特征包括:反蒙古样斜睑裂、右眼虹膜缺损、鼻梁凹陷、高腭弓、伸舌、小颌畸形和小阴茎。脑部磁共振成像(MRI)显示小脑蚓部轻度发育不全,透明隔正常。该婴儿对低血糖治疗有反应,病情稳定后出院。在进行细胞遗传学评估之前,该婴儿未被诊断为“4p三体综合征”或“17q单体综合征”。

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