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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Rossi, Elisa, Boeri, Laura, Morbini, Patrizia, Pagella, Fabio, Colombo, Andrea, Matti, Elina, Olivieri, Carla, Villanacci, Vincenzo, Minelli, Antonella, Buscarini, Elisabetta, Canzonieri, Cecilia, Danesino, Cesare
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 2010
Témata:
Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky