Sturge-Weber disease with unusual cerebral atrophy and hydrocephalus

European Journal of Paediatric Neurology

Volumn 3, Issue 5, 1999, Pages 227-229

  Campistol, J ^a,b   Garcia Cazorla A ^a   Gonzalez Campo C ^a  

^a HOSPITAL CLÍNIC   (Spain)

^b HOSPITAL SANT JOAN DE DÉU   (Spain)

Author keywords

Bilateral involvement; Brain atrophy; Diffuse angiomatosis; Hydrocephalus; Newborn; Sturge Weber disease

Indexed keywords

ARTICLE; BRAIN ATROPHY; CASE REPORT; CHILD; DISEASE ASSOCIATION; DISEASE SEVERITY; FEMALE; HUMAN; HYDROCEPHALUS; PRIORITY JOURNAL; SEIZURE; STURGE WEBER SYNDROME;

EID: 0032870422     PISSN: 10903798     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1090-3798(99)90086-7     Document Type: Article

References (5)

1. Yeakley JW, Woodside M, Fenstermacher MJ. Bilateral neonatal Sturge-Weber-Dimitri disease: CT and MRI findings. AJNR 1992; 13: 1179-1182.
2. Daniel W, Allen D. Cranial CT and MR in the Klippel-Trenaunay syndrome. AJNR 1992; 13: 291-294.
3. Fishman MA, Baram TZ. Megalencephaly due to impaired cerebral venous return in a Sturge-Weber variant syndrome. J Child Neurol 1986; 1: 115-118.
4. Maria LB, Neufeld JA, Rosainz LC. Central nervous system structure and function in Sturge-Weber syndrome: evidence of neurologic and radiologic progression. J Child Neurol 1998; 13: 606-618.
5. Coley SC, Britton J, Clarke A. Status epilepticus and venous infarction in Sturge-Weber syndrome. Child's Nerv Syst 1998; 14: 693-696.