Literature DB >> 589858

Central nervous system arteriovenous malformations in multiple generations of a family with hereditary hemorrhagic telangiectasia.

C R King, E W Lovrien, J Reiss.   

Abstract

Hereditary hemorrhagic telangiectasia is described in four generations of a kinship. The family is unique in that three generations manifest central nervous system vascular disease, which was pathologically confirmed in two generations. Genetic linkage was not identified for 32 genetic markers studied. The literature is reviewed for patients with central nervous system arteriovenous malformations and hereditary hemorrhagic telangiectasia. The pathogenesis of the disease is discussed, and therapeutic modalities are considered.

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Year:  1977        PMID: 589858     DOI: 10.1111/j.1399-0004.1977.tb00956.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  3 in total

Review 1.  Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms.

Authors:  C L Shovlin; M Letarte
Journal:  Thorax       Date:  1999-08       Impact factor: 9.139

2.  Unruptured intracranial arteriovenous malformations with hereditary haemorrhagic telangiectasia. Neurosurgical treatment or not?

Authors:  J W ter Berg; D W Dippel; J D Habbema; C J Westermann; C A Tulleken; J Willemse
Journal:  Acta Neurochir (Wien)       Date:  1993       Impact factor: 2.216

3.  Cerebral embolism--first manifestation of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia.

Authors:  R C Hewes; M Auster; R I White
Journal:  Cardiovasc Intervent Radiol       Date:  1985       Impact factor: 2.740

  3 in total

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