Results 61 to 70 of about 10,609 (274)
Journal of Ultrasound in Medicine, EarlyView.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 ...
Tomer Shwartz +6 more
wiley +1 more source
Case Report: A Rare Case of a Combination of Omphalocele With Umbilical Teratoma
Frontiers in Pediatrics, 2021 Omphalocele is a congenital malformation of the abdominal wall, which occurs with a frequency of 1–5,000 newborns. The prognosis of treatment often depends on the presence of concomitant malformations.
Ruslan Bilal +4 more
doaj +1 more source
Correlation between isolated sonographic finding of umbilical cord cyst and fetal anomalies [PDF]
, 2008 OBJETIVO: Correlacionar o achado ultra-sonográfico isolado de cisto de cordão umbilical com anomalias fetais, como cromossomopatias e alterações estruturais.
CERRI, Giovanni Guido +4 more
core +2 more sources
Breast Findings in Females With Beckwith–Wiedemann Syndrome
Pediatric Blood &Cancer, EarlyView.ABSTRACT Beckwith–Wiedemann syndrome (BWS) is an overgrowth condition caused by epigenetic defects on chromosome 11p15. Children with BWS have a predisposition to embryonal tumors such as Wilms tumor and hepatoblastoma. However, few reports of breast tumors in females with BWS have been published and the risk of malignancy and need for screening ...
Liron D. Grossmann +5 more
wiley +1 more source
Genetic analysis of Hedgehog signaling in ventral body wall development and the onset of omphalocele formation. [PDF]
PLoS ONE, 2011 An omphalocele is one of the major ventral body wall malformations and is characterized by abnormally herniated viscera from the body trunk. It has been frequently found to be associated with other structural malformations, such as genitourinary ...
Daisuke Matsumaru +6 more
doaj +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Objective To describe the implementation of whole genome sequencing (WGS) in prenatal diagnostics and outline the national guideline system facilitating this. Methods Clinical guidelines for WGS in prenatal diagnostics were developed and implemented by the Danish Fetal Medicine Society.
Ida Vogel +17 more
wiley +1 more source
Repair of giant omphalocele by component separation technique
Journal of Pediatric Surgery Case Reports, 2019 Giant omphalocele management has always been a challenge because of the large fascial defect and the associated anomalies. We managed successfully a neonate with giant omphalocele and no associated anomalies by delayed repair constituting escharotic ...
Mutua Irene, Swaleh Shahbal
doaj +1 more source
Onfalocele: análise de 33 casos. [PDF]
, 2001 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Arisa, Alessandro Mendes
core
LIMB BODY WALL COMPLEX IN TWO HETEROZYGOTIC TWINS: A CASE REPORT [PDF]
, 2011 Introdution. Limb-Body Wall Complex (LBWC) is a congenital defect which includes at least two of the following characteristics: abdominal and/or thoracic body wall defects, exencephaly or encephalocoele with or without craniofacial defects (56%) and ...
Angotti, R +4 more
core +1 more source
Vaginal Delivery in Cases of Prenatally Diagnosed Omphalocele: Feasibility and Outcomes
Prenatal Diagnosis, EarlyView.ABSTRACT Objective This study aimed to assess outcomes of fetuses with prenatally detected omphalocele and the frequency of successful vaginal delivery in pregnancies with suspected non‐lethal omphalocele and intended active neonatal management and its impact on neonatal outcome.
H. Heinrich +5 more
wiley +1 more source