Pulmonary artery hypertension in childhood: The transforming growth factor- β superfamily-related genes
Pulmonary artery hypertension (PAH) is very rare in childhood, and it can be divided into heritable, idiopathic drug- and toxin-induced and other disease (connective tissue disease, human immunodeficiency virus infection, portal hypertension, congenital heart disease, or schistosomiasis)-associated types. PAH could not be interpreted solely by pathophysiological theories. The impact of the transforming growth factor- β superfamily-related genes on the development of PAH in children remains to be clarified.
Source: Pediatrics and Neonatology - Category: Perinatology & Neonatology Authors: Shi-Min Yuan Tags: Review Article Source Type: research
More News: Cardiology | Child Development | Children | Genetics | Heart | Heart Disease | Hypertension | Pediatrics | Perinatology & Neonatology