Brain Arteriovenous Malformations associated with Hereditary Hemorrhagic Telangiectasia: Gene-Phenotype Correlations

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disease with a wide spectrum of vascular malformations involving multiple organs. Nine-16% of patients with HHT harbor brain arteriovenous malformations (AVMs), which can cause intracranial hemorrhage. Our objective was to...

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Main Authors: Nishida, Takeo, Faughnan, Marie E., Krings, Timo, Chakinala, Murali, Gossage, James R., Young, William L., Kim, Helen, Pourmohamad, Tony, Henderson, Katharine J., Schrum, Stacy D., James, Melissa, Quinnine, Nancy, Bharatha, Aditya, terBrugge, Karel G., White, Robert I.
Format: Artigo
Sprog:Inglês
Udgivet: 2012
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3610331/
https://ncbi.nlm.nih.gov/pubmed/22991266
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.35622
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