Sturge-Weber Syndrome Associated With Other Abnormalities
- 1 December 2005
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 62 (12) , 1924-1927
- https://doi.org/10.1001/archneur.62.12.1924
Abstract
Objective To develop hypotheses regarding the relationship between Sturge-Weber syndrome (SWS) and other abnormalities in a subset of patients. Design We retrospectively reviewed medical records in a group of 28 patients with SWS, noting the main features of SWS and accompanying unexpected abnormalities. We also conducted a literature review of abnormalities associated with SWS. Results Twenty-eight medical records of patients with SWS were reviewed. Of this number, we found 8 (29%, 2 female) patients who manifested other abnormalities. Our review of the literature uncovered 15 additional cases with associated abnormalities. Conclusions We hypothesize that the abnormalities associated with SWS suggest testable insights regarding pathogenesis and that chromosome 17p1-p13 may be a candidate region for genes involved with SWS. We also propose that some patients with SWS may have disorders of cholesterol biosynthesis or carbohydrate glycosylation.Keywords
This publication has 25 references indexed in Scilit:
- Coexistence of pleomorphic xanthoastrocytoma with Sturge-Weber syndrome: MRI featuresPediatric Radiology, 2005
- Increased Fibronectin Expression in Sturge-Weber Syndrome Fibroblasts and Brain TissuePediatric Research, 2003
- Evidence of somatic mosaicism in Sturge–Weber syndromeNeurology, 2002
- Locus for susceptibility for familial capillary malformation (‘port-wine stain’) maps to 5qEuropean Journal of Human Genetics, 2002
- Predominance of brain tumors in an extended Li-Fraumeni (SBLA) kindred, including a case of Sturge-Weber syndromeCancer, 2000
- Klippel-Trenaunay and Sturge-Weber syndrome with extensive Mongolian spots, hypoplastic larynx and subglottic stenosisClinical and Experimental Dermatology, 1988
- Lethal genes surviving by mosaicism: A possible explanation for sporadic birth defects involving the skinJournal of the American Academy of Dermatology, 1987
- Klippel-Trenaunay and Sturge-Weber Syndromes with Renal Hemangioma and Double Inferior Vena CavaJournal of Urology, 1986
- A giant meningioma of the fourth ventricle associated with Sturge-Weber diseaseActa Neurochirurgica, 1981
- Retinitis Pigmentosa Associated With Sturge-Weber SyndromeArchives of Ophthalmology (1950), 1966