Clinical findings of the phakomatoses: Sturge-Weber syndrome

Neurology

Volumn 66, Issue 4, 2006, Pages

  Quigg, Mark ^a   Rust, Robert S ^a   Miller, James Q ^a  

^a UNIVERSITY OF VIRGINIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; GLAUCOMA; HUMAN; INFANT; NEVUS FLAMMEUS; NUCLEAR MAGNETIC RESONANCE IMAGING; PHAKOMATOSIS; PRIORITY JOURNAL; STURGE WEBER SYNDROME; TRIGEMINAL NERVE; DIFFERENTIAL DIAGNOSIS; MALE; MENTAL DEFICIENCY; PARESIS; RADIOGRAPHY; SKULL;

DIAGNOSIS, DIFFERENTIAL; HUMANS; INFANT; MALE; MENTAL RETARDATION; NEUROCUTANEOUS SYNDROMES; PARESIS; PORT-WINE STAIN; SKULL; STURGE-WEBER SYNDROME;

EID: 33644991936     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000197789.72780.a9     Document Type: Article

References (1)

1. Tallman B, Tan OT, Morelli JG, et al. Location of port-wine stains and the likelihood of ophthalmic and/or central nervous system complications. Pediatrics 1991;87:323-327.