PAGOD syndrome

PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies.

Also known as: PAGOD syndrome, pulmonary hypoplasia-agonadism-dextrocardia-diaphragmatic hernia syndrome, Kennerknecht sorgo Oberhoffer syndrome, agonadism with multiple internal malformations, pulmonary hypoplasia, hypoplasia of the pulmonary artery, agonadism, omphalocele-diaphragmatic defect, and dextrocardia

5 clinical trials for this condition and its sub-types, 0 tagged with PAGOD syndrome itself.