| Literature DB >> 15820357 |
Antonio Donaire1, Mar Carreno, Nuria Bargalló, Xavier Setoaín, Rolando Agudo, Gisela Martín, Teresa Boget, Toni Raspall, Luis Pintor, Jordi Rumiá.
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.Entities:
Mesh:
Year: 2005 PMID: 15820357 DOI: 10.1016/j.yebeh.2005.02.002
Source DB: PubMed Journal: Epilepsy Behav ISSN: 1525-5050 Impact factor: 2.937