Literature DB >> 20582592

Neurocutaneous vascular syndromes.

Katherine B Puttgen1, Doris D M Lin.   

Abstract

There have been significant recent advances in the past several years in the field of neurocutaneous vascular syndromes, including the development of more stringent diagnostic criteria for PHACE syndrome, the renaming of macrocephaly-cutis marmorata telangiectatica congenita to macrocephaly-capillary malformation to accurately reflect the true nature of the syndrome, and discovery of new genetic mutations such as RASA-1. There have also been advances in the understanding and management of Sturge-Weber syndrome.PHACE syndrome is a constellation of neurologic, arterial, cardiac, ophthalmologic, and sternal abnormalities associated with infantile hemangiomas. PHACE is an acronym for Posterior fossa malformation, Hemangioma, Arterial anomalies, Coarctation of the aorta, Eye abnormalities. Some authors include an "S" for PHACE(S) to denote the association of ventral defects including Sternal clefting and Supraumbilical raphe.The accurate diagnosis and work-up of these patients require coordination of care across multiple disciplines, including neuroradiology, radiology, dermatology, neurology, surgery, and interventional radiology, among others.This paper is meant to update clinicians and researchers about important advances in these rare, important vascular syndromes, to improve care, and lay the foundation for future directions for research.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20582592     DOI: 10.1007/s00381-010-1201-3

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  48 in total

Review 1.  Sturge-Weber syndrome: a review.

Authors:  Kristin A Thomas-Sohl; Dale F Vaslow; Bernard L Maria
Journal:  Pediatr Neurol       Date:  2004-05       Impact factor: 3.372

Review 2.  Sturge-Weber syndrome and epilepsy: an argument for aggressive seizure management in these patients.

Authors:  Anne M Comi
Journal:  Expert Rev Neurother       Date:  2007-08       Impact factor: 4.618

Review 3.  Sturge-Weber syndrome revisited: the role of neuroradiology.

Authors:  P D Griffiths
Journal:  Neuropediatrics       Date:  1996-12       Impact factor: 1.947

4.  A prospective study of PHACE syndrome in infantile hemangiomas: demographic features, clinical findings, and complications.

Authors:  D W Metry; A N Haggstrom; B A Drolet; E Baselga; S Chamlin; M Garzon; K Horii; A Lucky; A J Mancini; B Newell; A Nopper; G Heyer; I J Frieden
Journal:  Am J Med Genet A       Date:  2006-05-01       Impact factor: 2.802

5.  Technetium-99m-HMPAO SPECT in Sturge-Weber syndrome.

Authors:  Z Bar-Sever; L P Connolly; P D Barnes; S T Treves
Journal:  J Nucl Med       Date:  1996-01       Impact factor: 10.057

6.  Consensus Statement on Diagnostic Criteria for PHACE Syndrome.

Authors:  Denise Metry; Geoffrey Heyer; Christopher Hess; Maria Garzon; Anita Haggstrom; Peter Frommelt; Denise Adams; Dawn Siegel; Karla Hall; Julie Powell; Ilona Frieden; Beth Drolet
Journal:  Pediatrics       Date:  2009-10-26       Impact factor: 7.124

7.  Ras GTPase-activating protein binds to Akt and is required for its activation.

Authors:  Yingzi Yue; Jaqueline Lypowy; Nadia Hedhli; Maha Abdellatif
Journal:  J Biol Chem       Date:  2004-01-05       Impact factor: 5.157

Review 8.  Update on Sturge-Weber syndrome: diagnosis, treatment, quantitative measures, and controversies.

Authors:  Anne M Comi
Journal:  Lymphat Res Biol       Date:  2007       Impact factor: 2.589

Review 9.  Macrocephaly-cutis marmorata telangiectatica congenita: report of six new patients and a review.

Authors:  Pablo Lapunzina; Alba Gairí; Alicia Delicado; M Angeles Mori; M Luisa de Torres; Anton Goma; Marcelo Navia; Isidora López Pajares
Journal:  Am J Med Genet A       Date:  2004-09-15       Impact factor: 2.802

10.  A novel mutation in RASA1 causes capillary malformation and limb enlargement.

Authors:  Dov Hershkovitz; Reuven Bergman; Eli Sprecher
Journal:  Arch Dermatol Res       Date:  2008-03-08       Impact factor: 3.017

View more
  7 in total

Review 1.  Neurocutaneous Disorders for the Practicing Neurologist: a Focused Review.

Authors:  Anna Carolina Paiva Costa T Figueiredo; Nikolas Mata-Machado; Matthew McCoyd; José Biller
Journal:  Curr Neurol Neurosci Rep       Date:  2016-02       Impact factor: 5.081

Review 2.  Multifocal arteriovenous malformations and facial nevus without leptomeningeal angioma: a variant form of Sturge-Weber syndrome? A case report and review of the literatures.

Authors:  In-Seok Bae; Hyeong-Joong Yi; Young Jun Lee
Journal:  Childs Nerv Syst       Date:  2012-09-30       Impact factor: 1.475

3.  CM-AVM syndrome in a neonate: case report and treatment with a novel flow reduction strategy.

Authors:  Emile Bacha; Jessica J Kandel; Gerald G Behr; Leonardo Liberman; Jocelyn Compton; Maria C Garzon; Kimberly D Morel; Christine T Lauren; Thomas J Starc; Stephen J Kovacs; Vincent Beltroni; Rachel Landres; Kwame Anyane-Yeboa; Philip M Meyers
Journal:  Vasc Cell       Date:  2012-11-20

4.  Sturge-Weber syndrome coexisting with autosomal dominant polycystic kidney disease.

Authors:  Mariusz Niemczyk; Renata Niemczyk; Monika Gradzik; Stanisław Niemczyk; Dariusz Kęcik; Leszek Pączek
Journal:  Int Urol Nephrol       Date:  2012-07-25       Impact factor: 2.370

Review 5.  Onyx(®) in endovascular treatment of cerebral arteriovenous malformations - a review.

Authors:  Maciej Szajner; Tomasz Roman; Justyna Markowicz; Małgorzata Szczerbo-Trojanowska
Journal:  Pol J Radiol       Date:  2013-07

Review 6.  Imaging More than Skin-Deep: Radiologic and Dermatologic Presentations of Systemic Disorders.

Authors:  Mehrzad Shafiei; Firoozeh Shomal Zadeh; Bahar Mansoori; Hunter Pyle; Nnenna Agim; Jorge Hinojosa; Arturo Dominguez; Cristina Thomas; Majid Chalian
Journal:  Diagnostics (Basel)       Date:  2022-08-19

7.  Pregnancy Tumor in a 31-Year-Old Female with a Facial Port-Wine Stain.

Authors:  Andrew Rockafellow; Whitney Florin; Elizabeth Philipone; David Koslovsky
Journal:  Case Rep Dent       Date:  2015-12-20
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.