Ultrasonography, Prenatal

Rene singolo congenito

Gruppo di lavoro sulle malformazioni congenite dei reni e delle vie urinarie della SINePe

2023/1 — pag. 21-30 — DOI

In recent years, several studies have been published on the prognosis of children with congenital solitary kidney (CSK), but a worldwide consensus on management and follow-up is still lacking. Recently, the Italian Society of Pediatric Nephrology has...

Se il rene non c’è... cerca ancora!

Favaretto E

2022/10 — pag. 215-215 — DOI

Cisti ovarica feto-neonatale complicata con torsione e autoamputazione

V. Genchi, N. Laforgia, F. Caroppo, M.P. Lanzilotto, G. Paradies

2019/5 — pag. 104-107

The paper reports a case of ovarian cyst discovered in pregnancy, complicated with torsion and subsequent auto-amputation and migration in contact with the sigma. It underlines the fundamental role of imaging, especially during pregnancy, and of ultr...

Pielectasie neonatiDosaggio della melatonina

2017/8 — pag. 533

Un vomito tanto precoce: la spia di un’atresia intestinale

G. Ferrara, T. Stampalija, D. Codrich, C. Simionato, A. Taddio, L. Travan

2016/4 — pag. 259-261

Small bowel atresia is a congenital obstruction of the lumen of the duodenum, jejunum or ileum and is one of the most common causes of neonatal bowel obstruction. It usually arises with vomiting in the first 48 h of life, but more and more frequen...

A proposito di red belly button: “quando l’uraco non si oblitera”

F. Matina, A. Federico, A. Costa, C. Mattina, D. Masaracchio

2014/4 — pag. 250-252

The urachus is a normal embryonic remnant of the primitive bladder dome and extends upward from the anterior dome of the bladder toward the umbilicus. Urachal remnant diseases are rare and manifest with nonspecific abdominal or urinary signs and sy...

Il destino dei nati pretermine

F. Mosca, M. Fumagalli, I. Sirgiovanni

2012/4 — pag. 221-226

The recent progresses made in perinatal medicine have determined an increase in the survival of newborns with lower and lower weight and earlier and earlier gestational age. Although neonatal mortality has decreased in the last few years, the incid...

Dalla diagnosi prenatale al management post natale delle malformazioni polmonari: suggerimenti per i pediatri

F. Gobbo, G. Pelizzo, J. Schleef

2010/2

Dalla diagnosi prenatale al management post-natale delle malformazioni polmonari

F. Gobbo, G. Pelizzo, J. Schleef

2010/2 — pag. 125-126

Congenital pulmonary airway malformations (CPAM) include a wide spectrum of developmental anomalies. Almost 50% of the cases are diagnosed in utero. These appear as hyperechoic, cystic or mixed lesions. Prenatal clinical course varies from seriou...

Follow-up a medio e lungo termine in bambini con megauretere non refluente: valutazione critica

R. Galiano, G. D’Onofrio, G. D’Ambrosio, V. Pascale, L. Giancotti, M. Baserga

2009/9 — pag. 597-598

Objectives - The purpose of our research was to assess the natural history of the non-refluxing, non-obstructive megaureter by means of a medium and long term follow-up. Methods - From 1992 to 2003 we observed 48 infants (37 males and 11 females)...

Sindrome acrocallosa in neonato (il contributo diagnostico dell'ecografia)

M. Budetta, I. Andreozzi

2000/1

Sindrome acrocallosa in neonato (il contributo diagnostico dell'ecografia

M. Budetta, I. Andreozzi

1999/10

Screening ecografico delle malformazioni fetali

D. Baronciani

1998/2 — pag. 111-112

Urologia malformativa: diagnosi prenatale e follow-up postnatale

A. Savanelli, S. Russo, G. Vallone, G. Esposito

1997/4 — pag. 233-239

The Authors report their experience on 100 newborns diagnosed in utero by ultrasound as having some kind of uropathy. The concordance between prenatal and postnatal diagnosis was 53%. Prenatal ultrasound was shown to be a very sensitive tool for...