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Metachronous Multiplicity of Spinal Cord Arteriovenous Fistula and Spinal Dural AVF in a Patient with Hereditary Haemorrhagic Telangiectasia

HHT (Hereditary Haemorrhagic Telangiectasia or Rendu Osler Weber disease) is a known autosomal dominant dysplasia. The first clinical presentation of HHT in a child may be a cerebral or spinal AVM. We present the case of a young boy with HHT who had a previous spinal cord AVF treated by surgical obl...

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Hlavní autoři: Ling, J.C.M., Agid, R., Nakano, S., Souza, M.P.S., Reintamm, G., TerBrugge, K.G.
Médium: Artigo
Jazyk:Inglês
Vydáno: Centauro S.r.l. 2005
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3403794/
https://ncbi.nlm.nih.gov/pubmed/20584440
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