Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9190469 | Epilepsy & Behavior | 2005 | 4 Pages |
Abstract
Fishman syndrome, also known as encephalocraniocutaneous lipomatosis (ECCL), is a rare, congenital neurocutaneous syndrome characterized by unilateral skin, eye, and brain abnormalities. Epileptic seizures and developmental delay are usually present. We report the clinical, radiological, and, for the first time, neurophysiological findings in a 24-year-old woman diagnosed with ECCL who was evaluated for epilepsy surgery. Functional magnetic resonance imaging revealed transfer of memory and language functions to the nonaffected hemisphere, providing evidence that functional reorganization and restoration of cognitive functions may occur in the context of extensive malformations, such as neurocutaneous syndromes.
Keywords
Related Topics
Life Sciences
Neuroscience
Behavioral Neuroscience
Authors
Antonio Donaire, Mar Carreno, Nuria Bargalló, Xavier SetoaÃn, Rolando Agudo, Gisela MartÃn, Teresa Boget, Toni Raspall, Luis Pintor, Jordi Rumiá,