Letter to Editor
Isolated Fetal Corpus Callosum Agenesis: Diagnosis and Management DifficultAchour Radhouane1*, Ksibi Imen2, Jammeli Nadia3, Aloui Nadia4, Kacem Samia1 and Neji Khaled1
- *Corresponding Author:
- Achour Radhouane
Maternity and Neonatalogy center tunis
Tel: + 21698549398
E-mail: [email protected]
Received date: September 21, 2016; Accepted date: October 12, 2016; Published date: October 20, 2016
Citation: Radhouane A, Imen K, Nadia J, Nadia A, Samia K, et al. (2016) Isolated Fetal Corpus Callosum Agenesis: Diagnosis and Management Difficult. J Neonatal Biol 5:234. doi:10.4172/2167-0897.1000234
Copyright: © 2016 Radhouane A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
The combined prevalence of partial or complete agenesis of the corpus callosum (ACC) is estimated at 0.02-0.5%.This common brain malformation mainly due to a prenatal abnormality commissuration. We report a case of diagnosis of isolated fetal CCA. Magnetic resonance imaging appears to be an important adjunct as it allows direct visualization. The prognosis in isolated agencies of the corpus callosum remains uncertain.