Immunohistochemical analysis of a merkeloma observed in a patient affected by hereditary haemorrhagic telangiectasia

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterised by epistaxis, telangiectases, and multiorgan vascular dysplasia. Mutations of the ENG and ACVRL1 genes cause at least 80% of cases. We report the first case of merkeloma found in a patient with HHT carrying...

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Autors principals: Rossi, Elisa, Boeri, Laura, Morbini, Patrizia, Pagella, Fabio, Colombo, Andrea, Matti, Elina, Olivieri, Carla, Villanacci, Vincenzo, Minelli, Antonella, Buscarini, Elisabetta, Canzonieri, Cecilia, Danesino, Cesare
Format: Artigo
Idioma:Inglês
Publicat: BMJ Publishing Group 2010
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3028296/
https://ncbi.nlm.nih.gov/pubmed/22315638
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.09.2009.2251
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