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hydroxyproline and Persistent Fetal Circulation Syndrome

hydroxyproline has been researched along with Persistent Fetal Circulation Syndrome in 1 studies

Hydroxyproline: A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
hydroxyproline : A proline derivative that is proline substituted by at least one hydroxy group.

Persistent Fetal Circulation Syndrome: 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).

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hassett, MJ1
Glick, PL1
Karamanoukian, HL1
Rossman, JE1
Wilcox, DT1
Azizkhan, RG1

Other Studies

1 other study available for hydroxyproline and Persistent Fetal Circulation Syndrome

ArticleYear
Pathophysiology of congenital diaphragmatic hernia. XVI: Elevated pulmonary collagen in the lamb model of congenital diaphragmatic hernia.
    Journal of pediatric surgery, 1995, Volume: 30, Issue:8

    Topics: Animals; Arterioles; Bronchi; Collagen; Disease Models, Animal; DNA; Elastin; Female; Gestational Ag

1995