Literature DB >> 17367610

Vascular malformations. Part II: associated syndromes.

Maria C Garzon1, Jennifer T Huang, Odile Enjolras, Ilona J Frieden.   

Abstract

UNLABELLED: Cutaneous vascular malformations are rare disorders representing errors in vascular development. These lesions occur much less commonly but are often confused with the common infantile hemangioma. It is important to properly diagnose vascular malformations because of their distinct differences in morbidity, prognosis and treatment. Vascular malformations may be associated with underlying disease or systemic anomalies. Several of these syndromes are well defined and can often be distinguished on the basis of the flow characteristics of the associated vascular malformation. LEARNING
OBJECTIVE: At the completion of this learning activity, participants should be able to better recognize underlying diseases or systemic anomalies that may be associated with vascular malformations. Participants should also better understand the various syndromes and conditions discussed and become more familiar with their management.

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Year:  2007        PMID: 17367610     DOI: 10.1016/j.jaad.2006.05.066

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  34 in total

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5.  Klippel-Trenaunay and Sturge-Weber overlapping syndrome in a Saudi boy.

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6.  General anesthesia in a patient with Parkes Weber syndrome with high-output cardiac failure due to multiple arteriovenous fistulas complicated by severe aortic regurgitation.

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Review 7.  Overgrowth syndrome in neonates: a rare case series with a review of the literature.

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Review 8.  Cutaneous lesions of the nose.

Authors:  Michael Sand; Daniel Sand; Christina Thrandorf; Volker Paech; Peter Altmeyer; Falk G Bechara
Journal:  Head Face Med       Date:  2010-06-04       Impact factor: 2.151

9.  Dominant inheritance and intra-familial variations in the association of Sturge-Weber and Klippel-Trenaunay-Weber syndromes.

Authors:  José Maria Pereira de Godoy; Agnes Cristina Fett-Conte
Journal:  Indian J Hum Genet       Date:  2010-01

10.  Maffucci syndrome with unilateral limb: a case report and review of the literature.

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