Literature DB >> 18555175

Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation.

Uğur Işik1, Seher Başaran, Tahir Dehgan, Memnune Apak.   

Abstract

We report on a 3-year-old boy with partial trisomy 8 p11.23-->pter and partial monosomy 4q34-->qter, associated with developmental delay, complete agenesis of the corpus callosum, and mild dysmorphic features. Although agenesis of the corpus callosum is not a rare finding among chromosomal abnormalities, partial trisomy 8p together with partial monosomy 4q, resulting from a maternal translocation, was not previously reported, to the best of our knowledge.

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Year:  2008        PMID: 18555175     DOI: 10.1016/j.pediatrneurol.2008.03.012

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  1 in total

1.  Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.

Authors:  Samin A Sajan; Liliana Fernandez; Sahar Esmaeeli Nieh; Eric Rider; Polina Bukshpun; Mari Wakahiro; Susan L Christian; Jean-Baptiste Rivière; Christopher T Sullivan; Jyotsna Sudi; Michael J Herriges; Alexander R Paciorkowski; A James Barkovich; Joseph T Glessner; Kathleen J Millen; Hakon Hakonarson; William B Dobyns; Elliott H Sherr
Journal:  PLoS Genet       Date:  2013-10-03       Impact factor: 5.917

  1 in total

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