Literature DB >> 18798309

Pure duplication 1q41-qter: further delineation of trisomy 1q syndromes.

Leslie Domenici Kulikowski1, Fernanda T S Bellucco, Sintia I Nogueira, Denise M Christofolini, Marilia de A C Smith, Claudia B de Mello, Decio Brunoni, Maria Isabel Melaragno.   

Abstract

Several authors have attempted to characterize the partial 1q trisomy syndrome, reporting clinical features such as mental retardation, macrocephaly, large fontanels, prominent forehead, broad flat nasal bridge, high-arched palate, micro/retrognathia, low-set ears, and cardiac defects. However, defining the partial trisomy 1q syndrome is difficult, because it is a rare chromosomal abnormality and in most instances the trisomy 1q is combined with partial monosomy of another autosomal segment. We report on the clinical and molecular cytogenetic study of a patient who presents pure partial 1q duplication. This is the first case of pure duplication 1q41-qter in the literature. 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18798309     DOI: 10.1002/ajmg.a.32510

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  10 in total

1.  Two rare cases of acute myeloid leukemia with t(8;16)(p11.2;p13.3) and 1q duplication: case presentation and literature review.

Authors:  Meng Liu; Yuan Ren; Xianfu Wang; Xianglan Lu; Ming Li; Young Mi Kim; Shibo Li; Lijun Zhang
Journal:  Mol Cytogenet       Date:  2020-08-25       Impact factor: 2.009

2.  Duplication 9p and their implication to phenotype.

Authors:  Roberta Santos Guilherme; Vera Ayres Meloni; Ana Beatriz Alvarez Perez; Ana Luiza Pilla; Marco Antonio Paula de Ramos; Anelisa Gollo Dantas; Sylvia Satomi Takeno; Leslie Domenici Kulikowski; Maria Isabel Melaragno
Journal:  BMC Med Genet       Date:  2014-12-20       Impact factor: 2.103

3.  Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up.

Authors:  Vera Ayres Meloni; Sylvia Satomi Takeno; Ana Luiza Pilla; Claudia Berlim de Mello; Maria Isabel Melaragno; Leslie Domenici Kulikowski
Journal:  Mol Cytogenet       Date:  2014-08-22       Impact factor: 2.009

4.  Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.

Authors:  Alicia Cervantes; Constanza García-Delgado; Fernando Fernández-Ramírez; Carolina Galaz-Montoya; Ariadna Berenice Morales-Jiménez; Karem Nieto-Martínez; Laura Gómez-Laguna; Judith Villa-Morales; Mónica Quintana-Palma; Jaime Berúmen; Susana Kofman; Verónica F Morán-Barroso
Journal:  BMC Med Genomics       Date:  2014-09-15       Impact factor: 3.063

5.  Rehabilitation Treatment of a Child Diagnosed With Duplication of 1q42-q44: A Case Report.

Authors:  Seong Woo Kim; Jiyong Kim; Ha Ra Jeon; Min Jung Park; Yoon Kim
Journal:  Ann Rehabil Med       Date:  2016-10-31

6.  Identification of IL11RA and MELK amplification in gastric cancer by comprehensive genomic profiling of gastric cancer cell lines.

Authors:  Danielle Queiroz Calcagno; Sylvia Santomi Takeno; Carolina Oliveira Gigek; Mariana Ferreira Leal; Fernanda Wisnieski; Elizabeth Suchi Chen; Taíssa Maíra Thomaz Araújo; Eleonidas Moura Lima; Maria Isabel Melaragno; Samia Demachki; Paulo Pimentel Assumpção; Rommel Rodriguez Burbano; Marília Cardoso Smith
Journal:  World J Gastroenterol       Date:  2016-11-21       Impact factor: 5.742

7.  A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements.

Authors:  Tomohiro Kohmoto; Nana Okamoto; Takuya Naruto; Chie Murata; Yuya Ouchi; Naoko Fujita; Hidehito Inagaki; Shigeko Satomura; Nobuhiko Okamoto; Masako Saito; Kiyoshi Masuda; Hiroki Kurahashi; Issei Imoto
Journal:  Mol Cytogenet       Date:  2017-04-28       Impact factor: 2.009

8.  Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qter.

Authors:  Hirokazu Morokawa; Motoko Kamiya; Keiko Wakui; Mikiko Kobayashi; Takashi Kurata; Kazuyuki Matsuda; Rie Kawamura; Hiroyuki Kanno; Yoshimitsu Fukushima; Yozo Nakazawa; Tomoki Kosho
Journal:  Hum Genome Var       Date:  2018-05-21

9.  Constitutional 763.3 Kb chromosome 1q43 duplication encompassing only CHRM3 gene identified by next generation sequencing (NGS) in a child with intellectual disability.

Authors:  Xiaofei Cheng; Qifang Yang; Jun Liu; Juan Ye; Huiying Xiao; Gaimei Zhang; Yuanyuan Pan; Xia Li; Ruifeng Hao; Yinfeng Li
Journal:  Mol Cytogenet       Date:  2019-04-17       Impact factor: 2.009

10.  Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings.

Authors:  Aixiang Luo; Dehua Cheng; Shimin Yuan; Haiyu Li; Juan Du; Yang Zhang; Chuanchun Yang; Ge Lin; Wenyong Zhang; Yue-Qiu Tan
Journal:  Mol Cytogenet       Date:  2018-04-04       Impact factor: 2.009

  10 in total

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