Results 171 to 180 of about 55,310 (326)
Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-CardioFacial syndrome) [PDF]
, 2005 Deletion 22q11.2 syndrome (Del22) (DiGeorge/Velo-Cardio-Facial syndrome) is characterized by congenital heart defect (CHD), palatal anomalies, facial dysmorphisms, neonatal hypocalcemia, immune deficit, speech and learning disabilities. CHD is present
Marino, Bonnie +3 more
core
Tetralogy of Fallot, left ventricular clot, aortic dissection: rare association
, 2017 Cases of uncorrected adult tetralogy of Fallot are rare and mostly manifest secondary to complications. A 30-year-old man presented with progressive breathlessness and severe chest discomfort.
Satya Sridhar Kale +3 more
core +1 more source
Tetralogy of Fallot and hypertrophic cardiomyopathy in a case of cardiofaciocutaneous syndrome
The Turkish Journal of Pediatrics, 2008 Cardiofaciocutaneous (CFC) syndrome is a rare disorder characterized by psychomotor and growth retardation, a typical facial dysmorphism, congenital heart defects, and ectodermal abnormalities.
Selman Vefa Yildirim +3 more
doaj
The Nakata index and McGoon ratio: correlation with the severity of pulmonary regurgitation after the repair of paediatric tetralogy of Fallot [PDF]
, 2023 Reza Abbaszadeh +7 more
openalex +1 more source
Need of transannular patch in tetralogy of Fallot surgery carries a higher risk of reoperation but has no impact on late survival: results of Fallot repair in Finland [PDF]
, 2014 Pekka Ylitalo +4 more
openalex +1 more source
Aortic Dilatation in Repaired Tetralogy of Fallot
, 2017 Béatrice Bonello +12 more
openalex +2 more sources
Increase in Cardiac Troponin I in a Lamb with Tetralogy of Fallot
, 2013 Elisa Barp Neuwald +6 more
openalex +2 more sources