Presentation of Dyke-Davidoff-Masson Syndrome in a 32-Year-Old Female: Report of a Rare Case With a Literature Review

Dyke-Davidoff-Masson syndrome (DDMS) is a rare congenital or acquired neurological disorder that most commonly affects the pediatric population but also rarely reported in adults. DDMS results from brain injury intrauterine early years of life. It characterized by prominent cortical sulci, hyperpneumatization frontal sinus, unilateral cerebral hemiatrophy with ventricular dilation, and associated bony thickness cranial vault. Seizures asymmetric hemiparesis are consistent findings facial asymmetry mental retardation widely reported. Herein, we report case 32-year-old female patient presenting history seizure right-sided hemiparesis. Neuroimaging showed encephalomalacia gliosis ex vacuo dilatation calvarial diploic space widening. Our unique sense our presented adulthood no signs seizures during childhood well-controlled on monotherapy. Given adult presentation unusual medical literature, will help physicians to keep high differential diagnoses such cases. Awareness clinical features imaging can facilitate timely accurate diagnosis, thereby enabling appropriate prompt management.