Literature DB >> 22718018

Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination.

Keiko Shimojima1, Nobuhiko Okamoto, Yume Suzuki, Mari Saito, Masato Mori, Tatanori Yamagata, Mariko Y Momoi, Hideji Hattori, Yoshiyuki Okano, Ken Hisata, Akihisa Okumura, Toshiyuki Yamamoto.   

Abstract

Subtelomeric deletions of 1q44 cause mental retardation, developmental delay and brain anomalies, including abnormalities of the corpus callosum (ACC) and microcephaly in most patients. We report the cases of six patients with 1q44 deletions; two patients with interstitial deletions of 1q44; and four patients with terminal deletions of 1q. One of the patients showed an unbalanced translocation between chromosome 5. All the deletion regions overlapped with previously reported critical regions for ACC, microcephaly and seizures, indicating the recurrent nature of the core phenotypic features of 1q44 deletions. The four patients with terminal deletions of 1q exhibited severe volume loss in the brain as compared with patients who harbored interstitial deletions of 1q44. This indicated that telomeric regions have a role in severe volume loss of the brain. In addition, two patients with terminal deletions of 1q43, beyond the critical region for 1q44 deletion syndrome exhibited delayed myelination. As the deletion regions identified in these patients extended toward centromere, we conclude that the genes responsible for delayed myelination may be located in the neighboring region of 1q43.

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Year:  2012        PMID: 22718018     DOI: 10.1038/jhg.2012.77

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  7 in total

1.  Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum.

Authors:  Mitesh Shetty; Ambika Srikanth; Jayarama Kadandale; Sridevi Hegde
Journal:  Mol Syndromol       Date:  2015-09-11

2.  Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.

Authors:  Ivan Y Iourov; Svetlana G Vorsanova; Oxana S Kurinnaia; Maria A Zelenova; Alexandra P Silvanovich; Yuri B Yurov
Journal:  Mol Cytogenet       Date:  2012-12-31       Impact factor: 2.009

3.  Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients.

Authors:  Nancy Choucair; Joelle Abou Ghoch; Sandra Corbani; Pierre Cacciagli; Cecile Mignon-Ravix; Nabiha Salem; Nadine Jalkh; Sandra El Sabbagh; Ali Fawaz; Tony Ibrahim; Laurent Villard; André Mégarbané; Eliane Chouery
Journal:  Mol Cytogenet       Date:  2015-04-09       Impact factor: 2.009

4.  Characteristics of rare and private deletions identified in phenotypically normal individuals.

Authors:  Keiko Shimojima; Toshiyuki Yamamoto
Journal:  Hum Genome Var       Date:  2017-09-14

5.  Infantile spasms related to a 5q31.2-q31.3 microdeletion including PURA.

Authors:  Keiko Shimojima; Nobuhiko Okamoto; Kayo Ohmura; Hiroaki Nagase; Toshiyuki Yamamoto
Journal:  Hum Genome Var       Date:  2018-03-29

6.  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

7.  Case Report: Identification of a de novo Microdeletion 1q44 in a Patient With Seizures and Developmental Delay.

Authors:  Yiehen Tung; Haiying Lu; Wenxin Lin; Tingting Huang; Samuel Kim; Guo Hu; Gang Zhang; Guo Zheng
Journal:  Front Genet       Date:  2021-05-20       Impact factor: 4.599

  7 in total

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