Ultraschall Med. 1999 Feb;20(1):19-21. (German)
[Echogenic intracardiac structures (golf ball phenomenon) as predictors of chromosome anomalies]
Bettelheim D, Ulm MR, Deutinger J, Bernaschek G.
Universitatsklinik fur Frauenheilkunde, Abteilung fur Pranatale Diagnostik und Therapie, Wien.
Echocardiographic Findings in Patients
Meeting Task Force Criteria for Arrhythmogenic Right Ventricular Dysplasia
New Insights From the Multidisciplinary Study of Right Ventricular Dysplasia
Danita M. Yoerger, MD,* Frank Marcus, MD,†Duane Sherrill, PHD,†Hugh Calkins, MD,‡
Jeffery A. Towbin, MD,§ Wojciech Zareba, MD, PHD, Michael H. Picard, MD,*
for the
Multidisciplinary Study of Right Ventricular Dysplasia Investigators
Boston, Massachusetts; Tucson, Arizona; Baltimore, Maryland; Houston, Texas; and Rochester, New York
OBJECTIVES
The purpose of this study was to quantify the echocardiographic abnormalities in probands
who were newly diagnosed with arrhythmogenic right ventricular dysplasia (ARVD).
BACKGROUND The diagnosis of ARVD remains challenging. The Multidisciplinary Study of Right
Ventricular Dysplasia was initiated to characterize the cardiac structural, clinical, and genetic
aspects of ARVD
La sindrome del cuore sinistro ipoplasico è caratterizzata da un ventricolo sinistro piccolo,
talvolta virtuale, stenosi critica o atresia delle valvole aortica e/o della mitrale e
ipoplasia dell’aorta ascendente e dell’arco dell’aorta, atrio sinistro piccolo,coartazione dell’aorta che
è la malformazione associata più frequente.
Rappresenta circa 1% di tutte le malformazioni cardiache congenite e, se non trattata,
ha la più alta mortalità nel primo mese di vita.
Unguarded tricuspid valvar orifice in the fetus
Kenny K. Wong; Duncan I. Farquharson; Walter J. Duncan
Cardiology in the Young, October 2004, vol. 14, no. 5, pp. 557-559(3)
Publisher: Greenwich Medical Media
Abstract:
Creazione in utero di un difetto nel setto atriale in feti con Sindrome del Cuore Sinistro Ipoplasico e setto atriale intatto o fortemente restrittivo.
Ultrasound Obstet Gynecol 2004; 24: 629–632
Published online in Wiley InterScience (www.interscience.wiley.com). DOI: 10.1002/uog.1753
Prenatal diagnosis of Shone’s syndrome: parental counseling and clinical outcome
N. ZUCKER, A. LEVITAS and E. ZALZSTEIN
Pediatric Cardiology Unit, Department of Pediatrics, Soroka University Medical Center, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel
KEYWORDS: fetal echocardiography; prenatal diagnosis; Shone’s syndrome
La sindrome di Shone comprende quattro anomalie :
1- una membrana sopravalvolare mitralica
2- mitrale a paracadute
3- stenosi subaortica (membranosa o muscolare)
4- coartazione aortica
Esiste anche una forma incompleta in cui si riconoscono solo due o tre componenti. Ha una scarsa prognosi chirurgica con una mortalità tra il 24-27% e richiede interventi multipli con una scarsa prognosi a distanza.
A study of congenital cardiac disease in a neonatal population – the validity of echocardiography undertaken by a neonatologist
Authors: Gregory R. Samson; Suresh R. Kumar
Source : Cardiology in the Young, December 2004, vol. 14, no. 6, pp. 585-593(9)
Publisher: Greenwich Medical Media
