Literature DB >> 17259353

Familial occurrence of brain arteriovenous malformations: a systematic review.

J van Beijnum1, H B van der Worp, H M Schippers, O van Nieuwenhuizen, L J Kappelle, G J E Rinkel, J W Berkelbach van der Sprenkel, C J M Klijn.   

Abstract

BACKGROUND: Brain arteriovenous malformations (BAVMs) are thought to be sporadic developmental vascular lesions, but familial occurrence has been described. We compared the characteristics of patients with familial BAVMs with those of patients with sporadic BAVMs.
METHODS: We systematically reviewed the literature on patients with familial BAVMs. Three families that were found in our centre were added. Age, sex distribution and clinical presentation of the identified patients were compared with those in population based series of patients with sporadic BAVMs. Furthermore, we calculated the difference in mean age at diagnosis of parents and children to study possible anticipation.
RESULTS: We identified 53 patients in 25 families with BAVMs. Mean age at diagnosis of patients with familial BAVMs was 27 years (range 9 months to 58 years), which was younger than in the reference population (difference between means 8 years, 95% CI 3 to 13 years). Patients with familial BAVMs did not differ from the reference populations with respect to sex or mode of presentation. In families with BAVMs in successive generations, the age of the child at diagnosis was younger than the age of the parent (difference between means 22 years, 95% CI 13 to 30 years), which suggests clinical anticipation.
CONCLUSIONS: Few patients with familial BAVMs have been described. These patients were diagnosed at a younger age than sporadic BAVMs whereas their mode of presentation was similar. Although there are indications of anticipation, it remains as yet unclear whether the described families represent accidental aggregation or indicate true familial occurrence of BAVMs.

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Year:  2007        PMID: 17259353      PMCID: PMC2117609          DOI: 10.1136/jnnp.2006.112227

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  51 in total

Review 1.  Familial occurrence of arteriovenous malformation of the brain.

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2.  Cerebral angiomata in an Icelandic family.

Authors:  H A KIDD; J N CUMINGS
Journal:  Lancet       Date:  1947-05-31       Impact factor: 79.321

Review 3.  Familial arteriovenous malformations in children.

Authors:  R J Brilli; A Sacchetti; S Neff
Journal:  Pediatr Emerg Care       Date:  1995-12       Impact factor: 1.454

4.  Hereditary neurocutaneous angiomatosis. Report of four cases.

Authors:  R Leblanc; D Melanson; R D Wilkinson
Journal:  J Neurosurg       Date:  1996-12       Impact factor: 5.115

5.  Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

Authors:  D W Johnson; J N Berg; M A Baldwin; C J Gallione; I Marondel; S J Yoon; T T Stenzel; M Speer; M A Pericak-Vance; A Diamond; A E Guttmacher; C E Jackson; L Attisano; R Kucherlapati; M E Porteous; D A Marchuk
Journal:  Nat Genet       Date:  1996-06       Impact factor: 38.330

6.  Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.

Authors:  K A McAllister; K M Grogg; D W Johnson; C J Gallione; M A Baldwin; C E Jackson; E A Helmbold; D S Markel; W C McKinnon; J Murrell
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7.  Familial subarachnoid hemorrhage: distinctive features and patterns of inheritance.

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8.  Central nervous system arteriovenous malformations with hereditary hemorrhagic telangiectasia: report of a family with three cases.

Authors:  C Kadoya; Y Momota; Y Ikegami; E Urasaki; S Wada; A Yokota
Journal:  Surg Neurol       Date:  1994-09

9.  The natural history of familial cavernous malformations: results of an ongoing study.

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Journal:  J Neurosurg       Date:  1994-03       Impact factor: 5.115

Review 10.  Familial arteriovenous malformations of the brain--two case reports.

Authors:  S Goto; M Abe; T Tsuji; K Tabuchi
Journal:  Neurol Med Chir (Tokyo)       Date:  1994-04       Impact factor: 1.742

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Review 1.  Endovascular management of arteriovenous malformations of the brain.

Authors:  Charles A Bruno; Philip M Meyers
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Review 2.  Role of embolization for cerebral arteriovenous malformations.

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Journal:  Methodist Debakey Cardiovasc J       Date:  2014 Oct-Dec

3.  Acute management of brain arteriovenous malformations.

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Journal:  Curr Treat Options Neurol       Date:  2015-05       Impact factor: 3.598

Review 4.  Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis.

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5.  Sudden death from ruptured intracranial vascular malformation.

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6.  Polymorphisms in ACVRL1 and endoglin genes are not associated with sporadic and HHT-related brain AVMs in Dutch patients.

Authors:  Kim Boshuisen; Manon Brundel; Carolien G F de Kovel; Tom G Letteboer; Gabriel J E Rinkel; Cornelis J J Westermann; Helen Kim; Ludmila Pawlikowska; Bobby P C Koeleman; Catharina J M Klijn
Journal:  Transl Stroke Res       Date:  2012-11-29       Impact factor: 6.829

Review 7.  Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformations.

Authors:  H Kim; D A Marchuk; L Pawlikowska; Y Chen; H Su; G Y Yang; W L Young
Journal:  Acta Neurochir Suppl       Date:  2008

8.  Genetic susceptibility to cerebrovascular disease: A systematic review.

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9.  EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations.

Authors:  Shantel Weinsheimer; Helen Kim; Ludmila Pawlikowska; Yongmei Chen; Michael T Lawton; Stephen Sidney; Pui-Yan Kwok; Charles E McCulloch; William L Young
Journal:  Circ Cardiovasc Genet       Date:  2009-08-22

10.  Genome-wide association study of sporadic brain arteriovenous malformations.

Authors:  Shantel Weinsheimer; Nasrine Bendjilali; Jeffrey Nelson; Diana E Guo; Jonathan G Zaroff; Stephen Sidney; Charles E McCulloch; Rustam Al-Shahi Salman; Jonathan N Berg; Bobby P C Koeleman; Matthias Simon; Azize Bostroem; Marco Fontanella; Carmelo L Sturiale; Roberto Pola; Alfredo Puca; Michael T Lawton; William L Young; Ludmila Pawlikowska; Catharina J M Klijn; Helen Kim
Journal:  J Neurol Neurosurg Psychiatry       Date:  2016-01-27       Impact factor: 10.154

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