Diseases [C] » Respiratory Tract Diseases [C08] » Lung Diseases » Hypertension, Pulmonary » Persistent Fetal Circulation Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Infant, Newborn, Diseases » Persistent Fetal Circulation Syndrome
Description
A syndrome of persistent PULMONARY HYPERTENSION in the newborn infant (INFANT, NEWBORN) without demonstrable HEART DISEASES. This neonatal condition can be caused by severe pulmonary vasoconstriction (reactive type), hypertrophy of pulmonary arterial muscle (hypertrophic type), or abnormally developed pulmonary arterioles (hypoplastic type). The newborn patient exhibits CYANOSIS and ACIDOSIS due to the persistence of fetal circulatory pattern of right-to-left shunting of blood through a patent ductus arteriosus (DUCTUS ARTERIOSUS, PATENT) and at times a patent foramen ovale (FORAMEN OVALE, PATENT). MeSH
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Approved Indicated Drugs (1)
Phase 4 Indicated Drugs (5)
Other Experimental Indicated Drugs (1)
Organization Involved with Phase 4 Indications (5)
Organization Involved with Phase 3 Indications (34)
Health Sciences Centre Foundation, Manitoba
Medical Research Council of Canada
National Center for Research Resources (NCRR)
National Institute of Child Health and Human Development (NICHD)
Organization Involved with Phase 2 Indications (4)
Organization Involved with Phase 1 Indications (3)
Organization Involved with Other Experimental Indications (4)
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UMLS Data
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