Sturge-Weber syndrome (SWS) is a rare, noninherited neurovascular disorder characterized by abnormal vasculature in the brain, skin, and eye. Patients with SWS characteristically have facial capillary malformation, also known as port-wine birthmark, a leptomeningeal vascular malformation seen on contrast-enhanced magnetic resonance imaging images, abnormal blood vessels in the eye, and glaucoma. Patients with SWS have impaired perfusion to the brain and are at high risk of venous stroke and stroke-like episodes, seizures, and both motor and cognitive difficulties. While the activating R183Q GNAQ somatic mutation is the most common somatic mutation underlying SWS, recent research also implicates that GNA11 and GNB2 somatic mutations are related to SWS. Recent retrospective studies suggest the use of low-dose aspirin and vitamin D in treatment for SWS and prospective drug trials have supported the usefulness of cannabidiol and Sirolimus. Presymptomatic treatment with low-dose aspirin and antiepileptic drugs shows promising results in delaying seizure onset in some patients. This review focuses on the latest progress in the field of research for Sturge-Weber syndrome and highlights directions for future research.
Keyphrases
- low dose
- contrast enhanced
- magnetic resonance imaging
- computed tomography
- high dose
- diffusion weighted
- copy number
- atrial fibrillation
- case report
- end stage renal disease
- magnetic resonance
- cardiovascular events
- resting state
- white matter
- signaling pathway
- diffusion weighted imaging
- chronic kidney disease
- soft tissue
- functional connectivity
- deep learning
- emergency department
- small cell lung cancer
- cross sectional
- machine learning
- cerebrospinal fluid
- prognostic factors
- coronary artery disease
- replacement therapy
- genome wide
- minimally invasive
- electronic health record
- patient reported
- gene expression
- anti inflammatory drugs