Congenital heart disease

Associazione VATER/VACTERL

Scupilliti S, Vancini A, Selicorni A

2025/5 — pag. 317-319 — DOI

Quando cuore e cervello sono connessi: ictus ischemico secondario a mixoma atriale sinistro

Bucciarell B, Spina E, Cappelletti D, Bianco F, Bucciarelli V, Merlino E, Fornaro M, Lionetti ME, Filippelli S

2025/2 — pag. 45-48 — DOI

The paper reports the case of a 17-year-old girl, apparently healthy, who presented to the Emergency Department with syncope, visual disturbances and vertigo during a walk. Neurological symptoms prompted an MRI, revealing subacute cerebellar ischemic...

Sindrome da microdelezione 22q11.2

Cazzaniga L, Scupilliti S, Selicorni A.

2024/5 — pag. 321-323 — DOI

Quando pensare alla sindrome di Noonan

Zuliani E

2024/1 — pag. 13-14 — DOI

Noonan syndrome is a pleomorphic genetic disorder that causes cardiovascular involvement in a high percentage of affected individuals. Care includes attentiveness to several comorbidities, some directly impacting cardiac management (bleeding diathese...

La sindrome di Noonan

Scupilliti S, Cianci P, Mariani M, Selicorni A.

2023/10 — pag. 657-659 — DOI

I vantaggi della correzione mininvasiva delle cardiopatie congenite riletti dopo 25 anni di esperienza

Cattapan C, Guariento A, Castaldi B, Sirico D, Scattolin F, Padalino M, Di Salvo G, Vida V

2023/9 — pag. 167-176 — DOI

Background - For many years the treatment of congenital heart disease has been performed through median sternotomy. Recently, the dimensions of the cutaneous incision have been reduced to optimize functional recovery and improve the aesthetic result....

Indovina chi? Uno dei due “mente”

Sette C, Ricci M.

2022/6 — pag. 396-398 — DOI

Two intriguing cases in which a somatic disease has been suspected are presented. The diagnosis of a functional disorder was confirmed for only one of them....

Quando lo scarso accrescimento è (anche) una questione di cuore

M.R. Arienzo, F. Angrisani

2020/26 — pag. 167-167 — DOI

Un minestrone preparato con il cuore

A. Iacono

2019/7 — pag. 449-451

Il binomio rivelatore: neutropenia e reticolo venoso marcato

G. Zanella

2018/7

La sindrome di Williams

A. Fornari, P. Cianci, A. Selicorni

2018/2 — pag. 111-113

La sindrome CHARGE

S. Tajè, P. Cianci, A. Selicorni

2017/9 — pag. 585-586

Elettrocardiogramma: ABC... e D per il pediatra

V. Gesuete

2017/4 — pag. 219-226

The paediatric electrocardiogram has particular features that distinguish it from that of an adult. Everyone needs to know them in order to interpret it correctly. A systematic approach that for example considers rhythm, heart rate, axis, and inter...

Il bambino con cardiopatia congenita nell’ambulatorio del pediatra

V. Gesuete, E. Parmeggiani, A. Ventura

2016/5 — pag. 291-296

Congenital heart disease is the most common type of congenital malformation at birth. Thanks to advances in diagnosis, therapy and the continuous development of surgical and interventional techniques, there has been a refinement in the treatment of...

Fetal alcohol syndrome sì, fetal alcohol syndrome no, fetal alcohol syndrome un cavolo!

L. Longoni, S. Maitz, A. Cereda, M. Mariani, F. Crosti, A. Selicorni

2016/4

Il cuore di Nico

B. Forini

2015/5

Le urgenze cardiologiche in età perinatale Parte I

U. Vairo, et al.

2004/4 — pag. 225-234

Congestive heart failure (CHF) is a clinical syndrome in which the heart is unable to pump enough blood to the body to meet its needs, to dispose of venous return adequately, or a combination of the two. CHF in the newborn usually result from conge...

Difetto interatriale Ostium Secundum chiusura transcatetere

U. Vairo, P. Appio, G. Argento, G. Adurno, G. Quaranta, M. V. Schiavo

2004/1

Difetto interatriale ostium secundum: chiusura transcatetere

2004/1 — pag. 56

Transcatheter closure of ostium secundum atrial septal defect with the Amplatzer Septal Occluder was performed in 40 patients (from March 2000 to December 2003) ranging in age from 2 to 67 years (median 23 years). Accurate assessment by transesoph...

L’adolescente e il giovane adulto con cardiopatia congenita

A. Benettoni, J. Somerville

2003/4 — pag. 243-249

The article addresses the needs and problems of grown-up congenital heart (GUCH) patients. The size of GUCH population is uncertain, but since 80-85% of patients born with congenital heart disease (CHD) now survive to adulthood (age 16 years), an a...

La sindrome CFC (Cardio-facio-cutaneous syndrome): un caso con piastrinopenia

A. Borrelli, G. Pinto

1999/3

Un soffio cardiaco scoperto in età scolare

G. Bosi

1997/3 — pag. 177-179

A cardiac murmur is a frequent finding in the school age child: on average, 1 out of 4 children presents with a murmur in this age group and in 1out of 50 of these children a “late onset” congenital heart disease is present. Pediatricians should...