Literature DB >> 25464110

21q21 deletion involving NCAM2: report of 3 cases with neurodevelopmental disorders.

Florence Petit1, Ghislaine Plessis2, Matthieu Decamp3, Jean-Marie Cuisset4, Moira Blyth5, Maria Pendlebury6, Joris Andrieux3.   

Abstract

Here we report three patients affected with neurodevelopmental disorders and harbouring 21q21 deletions involving NCAM2 gene. NCAM (Neural Cell Adhesion Molecule) proteins are involved in axonal migration, synaptic formation and plasticity. Poor axonal growth and fasciculation is observed in animal models deficient for NCAM2. Moreover, this gene has been proposed as a candidate for autism, based on genome-wide association studies. In this report, we provide a comprehensive molecular and phenotypical characterisation of three deletion cases giving additional clues for the involvement of NCAM2 in neurodevelopment.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  21q21 deletion; Array comparative genomic hybridization; Chromosomal abnormalities; Developmental delay; NCAM2

Mesh:

Substances:

Year:  2014        PMID: 25464110     DOI: 10.1016/j.ejmg.2014.11.004

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


  13 in total

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