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Scimitar syndrome, or congenital pulmonary venolobar syndrome, is a rare congenital heart defect characterized by anomalous venous return from the right lung (to the systemic venous drainage, rather than directly to the left atrium). [1] This anomalous pulmonary venous return can be either partial (PAPVR) or total (TAPVR).
Schöpf–Schulz–Passarge syndrome; Scimitar syndrome; Scott syndrome; Seaver Cassidy syndrome; Seckel syndrome; Second-impact syndrome; Secretan's syndrome; Seed dispersal syndrome; Senior–Løken syndrome; Sensenbrenner syndrome; Septo-optic dysplasia; Serkal syndrome; Serotonin syndrome; Serpentine fibula-polycystic kidney syndrome ...
Dressler syndrome: autoimmune inflammatory reaction secondary to MI. Edwards syndrome: genetic (Chromosome 18) Eisenmenger's syndrome: Ellis–van Creveld syndrome: Emanuel syndrome: HEC syndrome: Heyde's syndrome: Ho–Kaufman–Mcalister syndrome: Holt–Oram syndrome: ASD, and a first degree heart block. Hypoplastic left heart syndrome ...
The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).. This list continues the information at List of MeSH codes (C13).
Congenital stenosis of the vena cava is a sub-classification of the overarching spectrum of congenital heart disease involving the vessels surrounding the heart resulting in disruption to normal cardiovascular blood flow.
Scimitar Glacier, Washington State, United States; Scimitar oryx, a species of oryx; Scimitar syndrome, a rare congenital heart defect; Scimitar-billed woodcreeper, a bird species in the family Dendrocolaptinae; Scimitar-winged piha, a species of bird in the family Cotingidae; Scimitar, an entry-level cymbal series from manufacturer Zildjian
Causes include hypoxia, meconium aspiration, and respiratory distress syndrome. Left untreated, this can lead to hypoxic respiratory failure (HRF). [1] Decreased diameter of pulmonary vessels with hypertrophy of vessel walls: This has a poor prognosis, as it is a fixed abnormality.
Schaap–Taylor–Baraitser syndrome; Schaefer–Stein–Oshman syndrome; Schamberg's disease pigmentation disorder; Schamberg's disease; Scheie syndrome