Teaching Course in Morphology in Padua in May 2008
Basic Morphology Teaching Course will be held in Padua following the Venice Meeting.
You will find the final program with the registration form on AEPC web page.
Basic Morphology Teaching Course will be held in Padua following the Venice Meeting.
You will find the final program with the registration form on AEPC web page.
Joint meeting 43rdAnnual Meeting AEPC and 18th Spring meeting ECHSA
Venice Lido -Italy, May 21-24 2008
L’aneurisma e il diverticolo isolato del ventricolo destro sono rare anomalie congenite
il cui riscontro prenatale e’ eccezionalmente insolito.
1er SÉMINAIRE DE CARDIOLOGIE FŒTALE A PARIS
VENDREDI 1 ER FEVRIER 2008
SAMEDI 2 FEVRIER 2008
HÔPITAL ROBERT DEBRÉ
48, boulevard Sérurier
75935 PARIS CEDEX 19
The AEPC interventional working group is pleased to announce the second
TEACHING COURSE in pediatric and congenital INTERVENTIONAL CARDIAC
CATHETERISATION, which will take place on 4-5 april 2008, in Milan (Italy).
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.
XXXVII Congresso Nazionale della Societa’ Italiana di Cardiologia Pediatrica
Bergamo Centro Congressi Giovanni XXIII
8-10 Novembre 2007
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.
Vengono segnalati i Centri di Cardiochirurgia delle Cardiopatie Congenite dal neonato al giovane adulto.