Literature DB >> 10593557

Agenesis of the corpus callosum associated with DiGeorge-velocardiofacial syndrome: a case report and review of the literature.

N C Kraynack1, R W Hostoffer, N H Robin.   

Abstract

We report a patient with clinical and cytogenetic findings consistent with DiGeorge-velocardiofacial syndrome and agenesis of the corpus callosum. This patient represents the first report of a case of DiGeorge-velocardiofacial syndrome associated with such a central nervous system abnormality. This case, together with previous reports in the literature, suggests that structural brain abnormalities, and in particular abnormalities of the corpus callosum, are part of the complex syndrome associated with the chromosomal microdeletion 22q11.2. We suggest that the diagnosis of DiGeorge-velocardiofacial syndrome be entertained in patients with agenesis of the corpus callosum in the context of other common clinical features of this syndrome.

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Year:  1999        PMID: 10593557     DOI: 10.1177/088307389901401115

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  4 in total

1.  Periventricular heterotopia in common microdeletion syndromes.

Authors:  M van Kogelenberg; S Ghedia; G McGillivray; D Bruno; R Leventer; K Macdermot; J Nelson; L Nagarajan; J A Veltman; A P de Brouwer; R J McKinlay Gardner; H van Bokhoven; E P Kirk; S P Robertson
Journal:  Mol Syndromol       Date:  2010-01-08

Review 2.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Authors:  Daniel Paul Eisenberg; Mbemba Jabbi; Karen Faith Berman
Journal:  Neuroimage       Date:  2010-03-03       Impact factor: 6.556

Review 3.  Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.

Authors:  Daniel W Meechan; Thomas M Maynard; Eric S Tucker; Alejandra Fernandez; Beverly A Karpinski; Lawrence A Rothblat; Anthony-S LaMantia
Journal:  Prog Neurobiol       Date:  2015-04-09       Impact factor: 11.685

4.  Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions.

Authors:  Carrie E Bearden; Theo G M van Erp; Rebecca A Dutton; Agatha D Lee; Tony J Simon; Tyrone D Cannon; Beverly S Emanuel; Donna McDonald-McGinn; Elaine H Zackai; Paul M Thompson
Journal:  Cereb Cortex       Date:  2008-05-14       Impact factor: 5.357

  4 in total

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