Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5905057 | European Journal of Medical Genetics | 2011 | 4 Pages |
Abstract
To date, more than 100 cases with a deletion of chromosome 2q have been identified, although studies reporting small interstitial deletions involving the 2q24.2-q24.3 region are still rare. Here, we have described the genotype and the phenotype of a boy with a 5.3Â Mb de novo deletion in this region, identified by SNP array analysis. The selected region included 20 genes, of which 4 are prominently expressed in the brain. Their combined haplo-insufficiency could explain the main clinical features of this patient which included mental retardation, severe hypotonia, joint laxity and mild dysmorphic traits.
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Authors
Chiara Magri, Giovanna Piovani, Alba Pilotta, Traversa Michele, Fabio Buzi, Sergio Barlati,