Results 21 to 30 of about 10,836 (250)
Combining Detailed Fetal Anatomy Scanning in the NT Window Versus Early Second Trimester Scanning at 14-16 Weeks: A Non-Inferiority Study. [PDF]
Objectives First‐trimester ultrasound has evolved to incorporate a detailed fetal anatomy scan (FAS) with nuchal translucency (NT) screening. Many institutions use a 2‐visit protocol: NT followed by detailed FAS at 14–16 weeks. We aimed to evaluate whether integrating detailed FAS into the NT window (12 + 5 to 13 + 6 weeks) is non‐inferior in ...
Shwartz T +6 more
europepmc +2 more sources
Geographic clusters of congenital anomalies in Argentina [PDF]
Geographical clusters are defined as the occurrence of an unusual number of cases higher than expected in a given geographical area in a certain period of time.
Barbero, Pablo +7 more
core +1 more source
Perinatal omphalocele rupture is a rare occurrence. We present a case of a baby delivered at 35 weeks with a known giant omphalocele, transverse lie, and the omphalocele downward in the birth canal who suffered rupture of the omphalocele and liver injury
Maria E. Linnaus +4 more
doaj +1 more source
Management of giant omphalocele with intestinal perforation
Case of a male infant delivered at 36 weeks of gestational age and found to have a giant omphalocele, later complicated by intestinal perforation. A giant omphalocele is an omphalocele with an opening greater than 5 cm in diameter and containing the ...
Ritah Chumdermpadetsuk +2 more
doaj +1 more source
Prenatal diagnosis of fetal omphalocele by ultrasound: A comparison of two centuries
An omphalocele, a fetal abdominal defect, is a very important congenital anomaly. Prenatal diagnosis of fetal omphalocele is crucial to clinical management.
Yu-Ling Liang +6 more
doaj +1 more source
Background Patients with omphalocele, a midline abdominal wall defect at the umbilical cord base, have a low survival rate. However, the long-term outcomes of fetuses with prenatally diagnosed omphalocele have scarcely been studied.
Yanting Que +10 more
doaj +1 more source
Omphalocele can be associated with single gene disorders, neural tube defects, diaphragmatic defects, fetal valproate syndrome, and syndromes of unknown etiology.
Chih-Ping Chen
doaj +1 more source
Wandering spleen with a history of omphalocele is extremely rare. We encountered a male baby with wandering spleen associated with omphalocele. This case of wandering spleen in a neonate was diagnosed by ultrasound and computed tomography scans after ...
Daisuke Masui +11 more
doaj +1 more source
Multiple Haemangiomas, Diaphragmatic Eventration and Beckwith-Wiedemann Syndrome: An Unusual Association [PDF]
A 6-month-old girl with Beckwith-Wiedemann syndrome, multiple haemangiomas (axillary, laryngeal, pulmonary and hepatic) and diaphragmatic eventration was reported. All tumours responded to treatment with propranolol.
Borges, C +3 more
core +1 more source
Giant omphalocele treated with simple daily dressing changes
Omphalocele, also called exomphalos, is an anterior abdominal wall midline defect of variable size involving the umbilical ring containing the herniated viscera into a sac made up of peritoneum, amnion and Wharton's jelly. Giant omphalocele is an extreme
Jayalaxmi shripati Aihole
doaj +1 more source

