Literature DB >> 11807869

Sotos syndrome associated with a de novo balanced reciprocal translocation t(5;8)(q35;q24.1).

Kiyoshi Imaizumi1, Junko Kimura, Mari Matsuo, Kenji Kurosawa, Mitsuo Masuno, Norio Niikawa, Yoshikazu Kuroki.   

Abstract

We describe a de novo balanced reciprocal translocation between the long arms of chromosomes 5 and 8 [46,XX,t(5;8)(q35;q24.1)] in a 15-month-old girl with a typical Sotos syndrome phenotype. Involvement of the 5q35 region was previously reported (Maroun et al. [1994: Am J Med Genet 50:291-293]) as one of translocation breakpoints in the present patient. We suggest that the gene responsible for Sotos syndrome is located to a distal long-arm region of chromosome 5. Copyright 2001 Wiley-Liss, Inc.

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Year:  2002        PMID: 11807869     DOI: 10.1002/ajmg.10080

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


  7 in total

1.  NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes.

Authors:  Jenny Douglas; Sandra Hanks; I Karen Temple; Sally Davies; Alexandra Murray; Meena Upadhyaya; Susan Tomkins; Helen E Hughes; Trevor R P Cole; Nazneen Rahman
Journal:  Am J Hum Genet       Date:  2002-12-02       Impact factor: 11.025

2.  Precise detection of chromosomal translocation or inversion breakpoints by whole-genome sequencing.

Authors:  Toshifumi Suzuki; Yoshinori Tsurusaki; Mitsuko Nakashima; Noriko Miyake; Hirotomo Saitsu; Satoru Takeda; Naomichi Matsumoto
Journal:  J Hum Genet       Date:  2014-10-09       Impact factor: 3.172

3.  Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort.

Authors:  Kyungsoo Ha; Priya Anand; Jennifer A Lee; Julie R Jones; Chong Ae Kim; Debora Romeo Bertola; Jonathan D J Labonne; Lawrence C Layman; Wolfgang Wenzel; Hyung-Goo Kim
Journal:  Genes (Basel)       Date:  2016-11-09       Impact factor: 4.096

Review 4.  Genome sequencing and implications for rare disorders.

Authors:  Jennifer E Posey
Journal:  Orphanet J Rare Dis       Date:  2019-06-24       Impact factor: 4.123

5.  NSD1 mutations by HPV status in head and neck cancer: differences in survival and response to DNA-damaging agents.

Authors:  Cassie Pan; Said Izreig; Wendell G Yarbrough; Natalia Issaeva
Journal:  Cancers Head Neck       Date:  2019-07-08

6.  Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform.

Authors:  Liang Hu; Fan Liang; Dehua Cheng; Zhiyuan Zhang; Guoliang Yu; Jianjun Zha; Yang Wang; Qi Xia; Daoli Yuan; Yueqiu Tan; Depeng Wang; Yu Liang; Ge Lin
Journal:  Front Genet       Date:  2020-01-14       Impact factor: 4.599

Review 7.  Sotos syndrome.

Authors:  Geneviève Baujat; Valérie Cormier-Daire
Journal:  Orphanet J Rare Dis       Date:  2007-09-07       Impact factor: 4.123

  7 in total

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