Clinical and pathologic features of Sturge-Weber syndrome in patients with refractory epilepsy

CONCLUSIONS: Calcification of leptomeningeal arteries, focal cortical dysplasia, and GNAQ alteration are common features in SWS pathology. Patients with refractory epilepsy caused by SWS can achieve satisfactory seizure control after surgery, but seizure control was compromised in patients with comorbid HS.PMID:38217527 | DOI:10.1093/ajcp/aqad174
Source: American Journal of Clinical Pathology - Category: Pathology Authors: Source Type: research