CC BY-NC-ND 4.0 · Ibnosina Journal of Medicine and Biomedical Sciences 2015; 07(02): 56-58
DOI: 10.4103/1947-489X.210271
Case Report

Incidentally discovered colpocephaly and corpus callosum agenesis in asymptomatic elderly patient

Taofik Nasrat
Wayne State University Detroit Medical Center, Detroit, Michigan, USA
,
Navid Seraji-Bozoergzad
Wayne State University Detroit Medical Center, Detroit, Michigan, USA
› Author Affiliations

Colpocephaly is very rare anatomic finding in the brain manifested by occipital horns that are disproportionately enlarged in comparison with other parts of the lateral ventricles. It is usually diagnosed prenatally by ultrasound or in early childhood when the patient presents with delayed mile stones, seizures, mental retardation, motor and sensory deficit. We present a case of colpocephaly and corpus callosum agenesis that diagnosed in a sixty six years old African American woman that did not suffer from any seizures, cognitive, motor or sensory disability prior to her current admission.



Publication History

Received: 23 January 2014

Accepted: 04 September 2014

Article published online:
07 July 2022

© 2015. The Libyan Authority of Scientific Research and Technologyand the Libyan Biotechnology Research Center. All rights reserved. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License,permitting copying and reproductionso long as the original work is given appropriate credit. Contents may not be used for commercial purposes, oradapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India