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通过高分辨率染色体微阵列分析在中国一名患有猫眼综合征的男孩中鉴定出的一条新发小标记染色体(22)。

A De Novo sSMC (22) Characterized by High-Resolution Chromosome Microarray Analysis in a Chinese Boy with Cat-Eye Syndrome.

作者信息

Li Jinjie, Zhang Yue, Diao Yanjun, Li Rui, Jiang Liqing, Zhou Lei, Liu Jiayun, Duan Weixun, Yang Liu

机构信息

Department of Laboratory Medicine, Xijing Hospital, Air Force Military Medical University, Xi' an 710032, China.

Department of Cardiovascular Surgery, Xijing Hospital, Air Force Military Medical University, Xi'an 710032, China.

出版信息

Case Rep Genet. 2021 Feb 27;2021:8824184. doi: 10.1155/2021/8824184. eCollection 2021.

Abstract

We report a 15-year-old boy with cat-eye syndrome (CES) without short stature or intellectual disorder. The boy was confirmed by cytogenetic and high-resolution chromosome microarray analysis (CMA). The G-banding karyotype confirmed the de novo of the patient. Also, the CMA result showed 1.76 Mb tetrasomy of proximal 22Q11.1 ⟶ 22Q11.21 consistent with CES {arr22q11.1q11.21 (16,888,899-18,644,241) X4}, a typical small type I CES chromosome. The patient has many of the basic characteristics of CES; however, he is taller than his peers instead of shorter. It is rarely reported in the past since short stature is a common feature of this syndrome. Furthermore, the boy has no intellectual disorder and attends a normal school since he was six-year-old. What bothered him most were recurrent respiratory infections, retromicrognathia, and heart defects.

摘要

我们报告了一名15岁患有猫眼综合征(CES)的男孩,他没有身材矮小或智力障碍。该男孩通过细胞遗传学和高分辨率染色体微阵列分析(CMA)得到确诊。G显带核型证实了患者的新发突变。此外,CMA结果显示22号染色体长臂近端11.1⟶11.21区域存在1.76 Mb的四体重复,与CES相符{arr22q11.1q11.21(16,888,899 - 18,644,241)X4},这是一种典型的小型I型CES染色体。该患者具有CES的许多基本特征;然而,他比同龄人高,而非身材矮小。由于身材矮小是该综合征的常见特征,过去很少有此类报道。此外,该男孩没有智力障碍,自六岁起就就读于普通学校。最困扰他的是反复呼吸道感染、小颌后缩和心脏缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47c9/7937470/e00dd9b28f05/CRIG2021-8824184.001.jpg

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