Case Report
Case Report: Radiogenomic Insights into Corpus Callosum Dysgenesis with Hypoplastic Septum Pellucidum
Baby NM*
Department of Radiology, Government Medical College, Ernakulam, Kerala, India
*Corresponding author:Nikita Mary Baby, Senior Resident, Department of Radiology Government Medical College, Ernakulam, Kerala, India. E-mail Id: nikita92.nmb@gmail.com
Copyright: ©2025 Baby NM. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Article Information:Submission: 19/09/2024; Accepted: 20/12/2024; Published: 02/01/2025
Abstract
This case report presents a radiogenomic approach to a patient with MRI findings of Corpus Callosum Dysgenesis (CCD) and Hypoplastic Septum Pellucidum (HSP). By meticulously observing and documenting radiological data, we integrate these findings to identify the causative genetic mutations, predict the neurodevelopmental course, and guide treatment planning. This case and approach highlight the potential to leverage radiogenomics using routine MRI findings to improve therapeutic strategies.
Keywords:Corpus Callosum Dysgenesis; Hypoplastic Septum Pellucidum; Radiogenomics; Genetic Mutations; Neurodevelopmental Disorders; Magnetic Resonance Imaging (MRI).