| Literature DB >> 9446051 |
Abstract
Encephalocraniocutaneous lipomatosis (ECCL) is a congenital neurocutaneous disorder of the adipose tissue. The dominant features of the syndrome, include: unilateral cerebral malformation, ipsilateral scalp, face and eye lesions and convulsions beginning in infancy. The authors report a case of 13-year old girl with signs of ECCL syndrome treated surgically for to intractable epilepsy.Entities:
Mesh:
Year: 1997 PMID: 9446051
Source DB: PubMed Journal: Neurol Neurochir Pol ISSN: 0028-3843 Impact factor: 1.621