Parma Intern. Echo Meeting ( June 25-26-27 , 2008 )
Don Hagler ( Mayo Clinic ), Steve Sanders ( H. Pediatrico Bambino Gesu’, Roma )
and myself ( Universita’ di Parma ) are glad and proud to present the next Edition of
the Parma Echo Meeting.
Don Hagler ( Mayo Clinic ), Steve Sanders ( H. Pediatrico Bambino Gesu’, Roma )
and myself ( Universita’ di Parma ) are glad and proud to present the next Edition of
the Parma Echo Meeting.
The concept of the fetus as a patient should not be understood in terms of the independent moral status of the fetus, i.e., some feature(s) of the fetus that, independently of other entities e including the pregnant woman, the physician, and the state – generates obligations of others to it.
XXXVII Congresso Nazionale della Societa’ Italiana di Cardiologia Pediatrica
Bergamo Centro Congressi Giovanni XXIII
8-10 Novembre 2007
Aorto-ventricular tunnel is a congenital, extracardiac channel which connects the ascending aorta above the sinutubular junction to the cavity of the left, or (less commonly) right ventricle………………….>
Hypoplastic left heart syndrome(HLHS) refers to the abnormal development of the left-sided
cardiac structures, resulting in obstruction to blood flow from the left ventricular outflow tract. In
addition, the syndrome includes underdevelopment of the left ventricle, aorta, and aortic arch, as
well as mitral atresia or stenosis…………….>
Pentalogy of Cantrell is a rare congenital malformation
characterized by midline defects, resulting from
defective development in the septum transversum. The
constellation of findings includes deficiency of the
diaphragmatic pericardium, lower sternum, anterior
diaphragm, supraumbilical abdominal wall often
allowing an omphalocele as well as an intrapericardial
diaphragmatic hernia, and a cardiac lesion, most often
a ventricular septal defect. In severe cases, the
heart herniates through the diaphragmatic defect,
causing thoracoabdominal ectopia cordis. Other
associated congenital cardiac lesions may include an
atrial septal defect, pulmonary valve stenosis, tetralogy
of Fallot, dextrocardia, anomalous pulmonary venous
connection, tricuspid atresia, and truncus arteriosus.
La Fibroelastosi Endomiocardica (FEE) sia congenita che acquisita e’ una malattia dell’endocardio
rara e scarsamente compresa etiopatogenicamente e che progressivamente porta a scompenso cardiaco e morte fetale o postnatale.
Le caratteristiche istopatologiche della FEE sono la deposizione di collagene ed elastina nell’endocardio,
l’ipertrofia ventricolare e l’ispessimento dell’endocardio.
Fetal echocardiography at the time of the nuchal translucency scan
C. M. Lombardi 1 *, M. Bellotti 2, V. Fesslova 3, A. Cappellini 4
Presebtazione di alcune immagine ecocardiografiche Fetali e Postnatali
Vengono segnalati i Centri di Cardiochirurgia delle Cardiopatie Congenite dal neonato al giovane adulto.