The Aicardi-Goutières syndrome is an encephalopathy characterized by an arrest of psychomotor development in the first months of life, spastic tetraplegia spastic tetraplegia, abnormal movements and acquired microcephaly. Neuroimaging reveals calcifications of the basal ganglia a...
Open access
Research Article10.9734/ajpr/2022/v8i130235
Sturge-Weber syndrome (SWS), also known as encephalofacial angiomatosis, is a rare congenital neurocutaneous and ocular condition. It is characterized by two types of malformations: a congenital facial port-wine stain and a capillary-venous leptomeningeal angioma, typically homol...
Open access
Research Article10.9734/ajpr/2024/v14i4339