Literature DB >> 16877925

Sturge-Weber syndrome and associated congenital vascular disorders: a review.

Nirmal Nathan1, Seth R Thaller.   

Abstract

Sturge-Weber syndrome (SWS), Klippel-Trenaunay syndrome (KTS), and Parkes-Weber syndrome (PWS) represent a wide range of congenital vascular abnormality syndromes. Although many of the diagnostic criteria overlap for these syndromes, there are important differences among these diseases that carry important prognostic and therapeutic implications. This review attempts to clearly distinguish among SWS, KTS, and PWS, although loosely categorizing them as a family of congenital vascular disorders. A review of literature reveals that a variety of diagnostic tools exist that can help differentiate between the syndromes and assess risk for certain complications, which may help tailor various treatment modalities for a particular patient.

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Year:  2006        PMID: 16877925     DOI: 10.1097/00001665-200607000-00024

Source DB:  PubMed          Journal:  J Craniofac Surg        ISSN: 1049-2275            Impact factor:   1.046


  3 in total

1.  Wnt/beta-catenin signaling is required for CNS, but not non-CNS, angiogenesis.

Authors:  Richard Daneman; Dritan Agalliu; Lu Zhou; Frank Kuhnert; Calvin J Kuo; Ben A Barres
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-07       Impact factor: 11.205

2.  Bilateral Sturge-Weber and Phakomatosis Pigmentovascularis with Glaucoma, an Overlap Syndrome.

Authors:  Bharat Patil; Gautam Sinha; Bhagabat Nayak; Reetika Sharma; Sadhana Kumari; Tanuj Dada
Journal:  Case Rep Ophthalmol Med       Date:  2015-05-06

3.  Low concentration of rapamycin inhibits hemangioma endothelial cell proliferation, migration, and vascular tumor formation in mice.

Authors:  Ningning Zheng; Xudong Ding; Rabita Jahan
Journal:  Curr Ther Res Clin Exp       Date:  2014-11-11
  3 in total

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