Abstract
Malformations of the central nervous system (CNS) encompass a heterogeneous group of congenital anomalies that may be isolated or appear as part of a genetic syndrome. Advances in identifying the genetic etiology underlying many CNS malformation and syndromes have led to the current genetic-based classifications that allows us to better estimate prognosis and potential complications. Herein, we discuss the main genetic, clinical and radiological features and their implications for diagnostic testing and disease management
Original language | English |
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Pages (from-to) | 735-740 |
Number of pages | 6 |
Journal | Acta Medica Mediterranea |
Volume | 29 |
Publication status | Published - 2013 |
All Science Journal Classification (ASJC) codes
- General Medicine