Literature DB >> 16799912

Colpocephaly: a case report.

Surasak Puvabanditsin1, Eugene Garrow, Yuliya Ostrerov, Dumitru Trucanu, Maja Ilic, John V Cholenkeril.   

Abstract

Colpocephaly is an abnormal enlargement of the occipital horn of the lateral ventricle, also described as persistence of the fetal configuration of the lateral ventricles. Since it was first described, colpocephaly has been found in association with several abnormalities of the brain. Various etiologies have been postulated, including intrauterine/perinatal injuries, genetic disorders, and an error of morphogenesis. We report a new case of colpocephaly associated with absence of the corpus callosum and review the literature.

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Year:  2006        PMID: 16799912     DOI: 10.1055/s-2006-947161

Source DB:  PubMed          Journal:  Am J Perinatol        ISSN: 0735-1631            Impact factor:   1.862


  3 in total

1.  A rare case of colpocephaly with macrocephaly successfully treated with ventriculo-peritoneal shunting.

Authors:  Ashis Patnaik; Sudhansu S Mishra; Sanjib Mishra; Srikanta Das
Journal:  J Pediatr Neurosci       Date:  2012-05

2.  Attention Deficit Hyperactivity Disorder in a Patient With Congenital Mirror Movement Disorder and Colpocephaly.

Authors:  Selcen Yaroglu Kazanci
Journal:  Iran J Pediatr       Date:  2015-10-06       Impact factor: 0.364

3.  The defining pathology of the new clinical and histopathologic entity ACTA2-related cerebrovascular disease.

Authors:  Maria-Magdalena Georgescu; Marco da Cunha Pinho; Timothy E Richardson; Jose Torrealba; L Maximilian Buja; Dianna M Milewicz; Jack M Raisanen; Dennis K Burns
Journal:  Acta Neuropathol Commun       Date:  2015-12-04       Impact factor: 7.801

  3 in total

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