Literature DB >> 21095468

Pathogenesis of vascular anomalies.

Laurence M Boon1, Fanny Ballieux, Miikka Vikkula.   

Abstract

Vascular anomalies are localized defects of vascular development. Most of them occur sporadically (ie, there is no familial history of lesions, yet in a few cases clear inheritance is observed). These inherited forms are often characterized by multifocal lesions that are mainly small in size and increase in number with patients' age. The authors review the known (genetic) causes of vascular anomalies and call attention to the concept of Knudson's double-hit mechanism to explain incomplete penetrance and large clinical variation in expressivity observed in inherited vascular anomalies. The authors also discuss the identified pathophysiological pathways involved in vascular anomalies and how it has opened the doors toward a more refined classification of vascular anomalies and the development of animal models that can be tested for specific molecular therapies.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21095468      PMCID: PMC3031181          DOI: 10.1016/j.cps.2010.08.012

Source DB:  PubMed          Journal:  Clin Plast Surg        ISSN: 0094-1298            Impact factor:   2.017


  95 in total

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Authors:  M Vikkula; L M Boon; K L Carraway; J T Calvert; A J Diamonti; B Goumnerov; K A Pasyk; D A Marchuk; M L Warman; L C Cantley; J B Mulliken; B R Olsen
Journal:  Cell       Date:  1996-12-27       Impact factor: 41.582

2.  Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas.

Authors:  S Laberge-le Couteulx; H H Jung; P Labauge; J P Houtteville; C Lescoat; M Cecillon; E Marechal; A Joutel; J F Bach; E Tournier-Lasserve
Journal:  Nat Genet       Date:  1999-10       Impact factor: 38.330

3.  A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.

Authors:  L M Boon; P Brouillard; A Irrthum; L Karttunen; M L Warman; R Rudolph; J B Mulliken; B R Olsen; M Vikkula
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

4.  Allelic and locus heterogeneity in inherited venous malformations.

Authors:  J T Calvert; T J Riney; C D Kontos; E H Cha; V G Prieto; C R Shea; J N Berg; N C Nevin; S A Simpson; K A Pasyk; M C Speer; K G Peters; D A Marchuk
Journal:  Hum Mol Genet       Date:  1999-07       Impact factor: 6.150

5.  A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.

Authors:  D W Johnson; J N Berg; C J Gallione; K A McAllister; J P Warner; E A Helmbold; D S Markel; C E Jackson; M E Porteous; D A Marchuk
Journal:  Genome Res       Date:  1995-08       Impact factor: 9.043

6.  Association of Krev-1/rap1a with Krit1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-22.

Authors:  I Serebriiskii; J Estojak; G Sonoda; J R Testa; E A Golemis
Journal:  Oncogene       Date:  1997-08-28       Impact factor: 9.867

7.  Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia.

Authors:  C L Shovlin; J M Hughes; J Scott; C E Seidman; J G Seidman
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

8.  FAP48, a new protein that forms specific complexes with both immunophilins FKBP59 and FKBP12. Prevention by the immunosuppressant drugs FK506 and rapamycin.

Authors:  B Chambraud; C Radanyi; J H Camonis; K Shazand; K Rajkowski; E E Baulieu
Journal:  J Biol Chem       Date:  1996-12-20       Impact factor: 5.157

9.  An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 families.

Authors:  P Labauge; O Enjolras; J J Bonerandi; S Laberge; M Dandurand; J M Joujoux; E Tournier-Lasserve
Journal:  Ann Neurol       Date:  1999-02       Impact factor: 10.422

10.  Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations.

Authors:  F Bergametti; C Denier; P Labauge; M Arnoult; S Boetto; M Clanet; P Coubes; B Echenne; R Ibrahim; B Irthum; G Jacquet; M Lonjon; J J Moreau; J P Neau; F Parker; M Tremoulet; E Tournier-Lasserve
Journal:  Am J Hum Genet       Date:  2004-11-12       Impact factor: 11.025

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  13 in total

1.  Intralesional diode laser pretreatment facilitates surgery for orbital venous malformations: initial experience with 23 consecutive patients.

Authors:  Minyue Xie; Tianyuan Li; Yingxiu Luo; Yinwei Li; Yefei Wang; Xianqun Fan; Ludwig M Heindl; Renbing Jia
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2.  Multimodality imaging of vascular anomalies.

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Journal:  Pediatr Radiol       Date:  2013-03-12

Review 3.  Pathogenesis of infantile haemangioma.

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Journal:  Br J Dermatol       Date:  2013-07       Impact factor: 9.302

4.  Protein expression, characterization and activity comparisons of wild type and mutant DUSP5 proteins.

Authors:  Jaladhi Nayak; Adam J Gastonguay; Marat R Talipov; Padmanabhan Vakeel; Elise A Span; Kelsey S Kalous; Raman G Kutty; Davin R Jensen; Phani Raj Pokkuluri; Daniel S Sem; Rajendra Rathore; Ramani Ramchandran
Journal:  BMC Biochem       Date:  2014-12-18       Impact factor: 4.059

5.  Combined Lymphedema and Capillary Malformation of the Lower Extremity.

Authors:  Reid A Maclellan; Gulraiz Chaudry; Arin K Greene
Journal:  Plast Reconstr Surg Glob Open       Date:  2016-02-10

6.  Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases.

Authors:  Roel W Ten Broek; Astrid Eijkelenboom; Carine J M van der Vleuten; Eveline J Kamping; Marleen Kets; Bas H Verhoeven; Katrien Grünberg; Leo J Schultze Kool; Bastiaan B J Tops; Marjolijn J L Ligtenberg; Uta Flucke
Journal:  Genes Chromosomes Cancer       Date:  2019-02-11       Impact factor: 5.006

7.  RASA1 functions in EPHB4 signaling pathway to suppress endothelial mTORC1 activity.

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8.  A frog in my throat doctor, well perhaps a tadpole? An interesting case of a laryngeal arteriovenous malformation.

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Journal:  BMJ Case Rep       Date:  2020-10-04

9.  Facial and Scalp Swelling in the Pediatric Population With Hemophilia: A Diagnosis Pitfall.

Authors:  W Widjaja; S Aggarwala; F Ballieux; J Vandervord
Journal:  Eplasty       Date:  2016-04-28

10.  Sirolimus is efficacious in treatment for extensive and/or complex slow-flow vascular malformations: a monocentric prospective phase II study.

Authors:  Jennifer Hammer; Emmanuel Seront; Steven Duez; Sophie Dupont; An Van Damme; Sandra Schmitz; Claire Hoyoux; Caroline Chopinet; Philippe Clapuyt; Frank Hammer; Miikka Vikkula; Laurence M Boon
Journal:  Orphanet J Rare Dis       Date:  2018-10-29       Impact factor: 4.123

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