Literature DB >> 12210324

Duplication of 8p23.2: a benign cytogenetic variant?

Naoki Harada1, Jun Takano, Tatsuro Kondoh, Hirofumi Ohashi, Tomonobu Hasegawa, Hirobumi Sugawara, Tomoko Ida, Ko-ichiro Yoshiura, Tohru Ohta, Tatsuya Kishino, Tadashi Kajii, Norio Niikawa, Naomichi Matsumoto.   

Abstract

We describe a duplication of the 8p23.2 band in seven individuals from four families. The duplication was recognizable as an enlarged 8p23.2 band on G-banded chromosomes at the 550 band level. It was transmitted from a parent to offspring in three of the four families in which both parents were karyotyped. Each proband in the four families had the enlarged band and showed various phenotypic abnormalities, but the abnormalities were inconsistent. Chromosomal and interphase fluorescence in situ hybridization (FISH) analysis of the enlarged band region defined a 2.5-Mb duplicated segment common to all seven individuals studied. Interphase FISH analysis of peripheral blood lymphocytes from 50 unrelated normal individuals showed the duplication in three individuals. In view of these findings, it is most likely that the 8p23.2 duplication we described is a normal variant. Copyright 2002 Wiley-Liss, Inc.

Mesh:

Year:  2002        PMID: 12210324     DOI: 10.1002/ajmg.10584

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

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4.  Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficulties.

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Journal:  Eur J Hum Genet       Date:  2008-08-20       Impact factor: 4.246

5.  A 9-year-old-girl with Phelan McDermid Syndrome, who had been diagnosed with an autism spectrum disorder.

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6.  Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2.

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7.  Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family.

Authors:  Ying Peng; Shuting Yang; Hui Xi; Jiancheng Hu; Zhengjun Jia; Jialun Pang; Jing Liu; Wenxian Yu; Chengyuan Tang; Hua Wang
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8.  Cri-Du-Chat Syndrome: Clinical Profile and Chromosomal Microarray Analysis in Six Patients.

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  8 in total

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