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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Vydáno v:BMC Med Genet
Hlavní autoři: Dello Russo, Patrizia, Franzoni, Alessandra, Baldan, Federica, Puppin, Cinzia, De Maglio, Giovanna, Pittini, Carla, Cattarossi, Luigi, Pizzolitto, Stefano, Damante, Giuseppe
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2015
Témata:
Case Report
On-line přístup: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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