vigabatrin has been researched along with Sturge-Weber Syndrome in 1 studies
Sturge-Weber Syndrome: A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Buchanan, N | 1 |
| Kearney, B | 1 |
1 other study available for vigabatrin and Sturge-Weber Syndrome
| Article | Year |
|---|---|
Vigabatrin in the Sturge Weber syndrome.
Topics: Adult; Aminocaproates; Anticonvulsants; Child, Preschool; Epilepsies, Partial; Female; Humans; Male; | 1993 |