Am J Perinatol 2006; 23(5): 295-298
DOI: 10.1055/s-2006-947161
Copyright © 2006 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA.

Colpocephaly: A Case Report

Surasak Puvabanditsin1 , Eugene Garrow2 , Yuliya Ostrerov1 , Dumitru Trucanu1 , Maja Ilic1 , John V. Cholenkeril3
  • 1Department of Pediatrics, University of Medicine and Dentistry of New Jersey, Newark, New Jersey
  • 2Department of Surgery, SUNY Downstate Medical Center, Brooklyn, New York
  • 3Department of Radiology, University of Medicine and Dentistry of New Jersey, Newark, New Jersey
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Publikationsdatum:
23. Juni 2006 (online)

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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.

REFERENCES

Surasak PuvabanditsinM.D. 

Department of Pediatrics, Jersey City Medical Center

355 Grand Street, Jersey City, NJ 07302