Literature DB >> 16602035

A case of partial trisomy of chromosome 8p associated with autism.

Katerina Papanikolaou1, Elena Paliokosta, Jolanda Gyftodimou, Gerassimos Kolaitis, Sofia Vgenopoulou, Catherine Sarri, John Tsiantis.   

Abstract

We report on a case of a 6-year-old female with partial trisomy 8p(21-23) associated with autism, mild dysmorphic features, and moderate learning disability. Although mental retardation is a common finding in patients with mosaic trisomy 8 or partial trisomy of various regions of chromosome 8, only two cases associated with autism have been reported so far. Also, in our case clinical manifestations were mild compared to other patients with duplication of the same region of chromosome 8. Although there has been no strong evidence for linkage on chromosome 8 in any of the genome-wide linkage studies so far, the possibility that this segment includes genes involved in the etiology of autism should be further explored.

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Year:  2006        PMID: 16602035     DOI: 10.1007/s10803-006-0104-3

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN: 0162-3257


  33 in total

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1.  Prolonged pancytopenia in a gene therapy patient with ADA-deficient SCID and trisomy 8 mosaicism: a case report.

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3.  A novel 6.14 Mb duplication of chromosome 8p21 in a patient with autism and self mutilation.

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Review 4.  Glutamatergic candidate genes in autism spectrum disorder: an overview.

Authors:  Andreas G Chiocchetti; Hanna S Bour; Christine M Freitag
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5.  Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficulties.

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6.  Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations.

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7.  PSD-Zip70 Deficiency Causes Prefrontal Hypofunction Associated with Glutamatergic Synapse Maturation Defects by Dysregulation of Rap2 Activity.

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8.  Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.

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9.  Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.

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Journal:  BMC Genomics       Date:  2016-03-01       Impact factor: 3.969

10.  De novo 8p21.3→ p23.3 Duplication With t(4;8)(q35;p21.3) Translocation Associated With Mental Retardation, Autism Spectrum Disorder, and Congenital Heart Defects: Case Report With Literature Review.

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Journal:  Front Pediatr       Date:  2020-07-08       Impact factor: 3.418

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