A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosis

BACKGROUND: Pulmonary capillary hemangiomatosis (PCH) is an uncommon pulmonary disorder, with variable clinical features depending on which lung structure is affected, and it is usually linked to pulmonary arterial hypertension. Congenital PCH has been very rarely described and, so far, the only cau...

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Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: Dello Russo, Patrizia, Franzoni, Alessandra, Baldan, Federica, Puppin, Cinzia, De Maglio, Giovanna, Pittini, Carla, Cattarossi, Luigi, Pizzolitto, Stefano, Damante, Giuseppe
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2015
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4605103/
https://ncbi.nlm.nih.gov/pubmed/26462560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-015-0241-7
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