Literature DB >> 22669037

A 4.5 Mb terminal deletion of chromosome 12p helps further define a psychosis-associated locus.

Hilda Vargas1, Gail Beldia, William Korosh, Vicki Sudhalter, Anwar Iqbal, Jose Arturo Sanchez-Lacay, Milen Velinov.   

Abstract

A 12 year-old girl presented with cognitive disability and dysmorphic features. Chromosome microarray analysis revealed a de novo, approximately 4.5 Mb terminal deletion of the short arm of chromosome 12 at 12p13.33 region: chr12:100712-4607067. At 13 years this patient developed psychotic manifestations and was admitted to a psychiatric department for treatment. She started hearing voices, talking to herself and laughing without reason. We have previously reported a male individual with psychotic manifestations and a larger (6.2 Mb) terminal deletion in the same chromosomal region. The present case along with previous reports, define a 2 Mb region on chromosome 12p, where a psychosis-associated gene may be located. Included in this psychosis-associated area are 18 OMIM listed genes.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.

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Year:  2012        PMID: 22669037     DOI: 10.1016/j.ejmg.2012.04.012

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  3 in total

1.  Small bowel malrotation in distal 15q duplication: evidence for a rare association.

Authors:  Brooke M McLaughlin; Robert B Hufnagel; Howard M Saal
Journal:  Clin Dysmorphol       Date:  2015-04       Impact factor: 0.816

2.  12p deletion spectrum syndrome: a new case report reinforces the evidence regarding the potential relationship to autism spectrum disorder and related developmental impairments.

Authors:  Marcio Leyser; Bruno Leonardo Dias; Ana Luiza Coelho; Marcio Vasconcelos; Osvaldo J M Nascimento
Journal:  Mol Cytogenet       Date:  2016-10-04       Impact factor: 2.009

Review 3.  Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33-p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review.

Authors:  Ji Yoon Han; Joonhong Park
Journal:  Genes (Basel)       Date:  2021-06-29       Impact factor: 4.096

  3 in total

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