Results 61 to 70 of about 14,608 (291)

15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies

Case Reports in Pediatrics, 2018
Background. Omphalocele is a rare congenital abdominal wall defect. It is frequently associated with genetic abnormality and other congenital anomalies, although isolated omphalocele cases do exist.
Hui-Fang Zhou, Christopher J. O’Conor, Chiraag Gangahar, Louis P. Dehner   +3 more
doaj   +1 more source

Giant Isolated Omphalocele: Role of Prenatal Diagnosis in Prognostic Asessment and Perinatal Management

Case Reports in Medicine, 2020
Omphalocele is a congenital malformation of the abdominal wall consisting of a protrusion of the abdominal contents at the base of the umbilical cord. It has a high association with genetic and structural defects; however, if the latter is ruled out, its
A. M. Cubo, M. V. Lapresa Alcalde, I. Gastaca, M. Rodriguez-Martin, M. C. Martín Seisdedos, M. V. R. Velasco Ayuso, R. C. Cebrián Muiños, J. Sayagués   +7 more
semanticscholar   +1 more source

Congenital anomalies in low- and middle-income countries: the unborn child of global surgery. [PDF]

, 2014
Surgically correctable congenital anomalies cause a substantial burden of global morbidity and mortality. These anomalies disproportionately affect children in low- and middle-income countries (LMICs) due to sociocultural, economic, and structural ...
AF Uba, AL Christianson, AR Measham, B Nandi, BC Warf, CJL Murray, D Adeyemi, D Ozgediz, D Ozgediz, D Poenaru, Diana L. Farmer, Doruk Ozgediz, DPJ Poenaru, DS Corlew, E Tefera, EE Ugiagbe, G Shah, GP Hadley, H Higashi, J Manson, J Rohana, J Sekabira, JA Salomon, JI Hoffman, KW Rattray, L Finer, L Mo-suwan, LB Chirdan, LB Chirdan, LC Nacul, M Peyvasteh, MADMS Islam, MJ Poley, MNH Toro, Nicole A. Sitkin, O Adejuyigbe, P Farmer, P Wickramasinghe, Peter Donkor, PL Bernier, S Agarwala, S Askarpour, S Bickler, S Mhando, SB Goksan, SO Ekenze, SO Ekenze, SW Bickler, SW Bickler, T Ozdogan, V Wu, VB Penchaszadeh, VK Wu, World Health Organization   +53 more
core   +3 more sources

Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies

Taiwanese Journal of Obstetrics & Gynecology, 2014
Objective: We describe a prenatal ultrasonography diagnosis of omphalocele and symbrachydactyly in a fetus and review the literature on prenatal diagnosis of 9p terminal chromosomal deletions.
Wen-Chien Hou, Chih-Ping Chen, Kwei-Shuai Hwang, Ying-Chieh Chen, Yu-Ju Lai, Chau-Yang Tien, Her-Young Su   +6 more
doaj   +1 more source

Severity of effect considerations regarding the use of mutation as a toxicological endpoint for risk assessment: A report from the 8th International Workshop on Genotoxicity Testing (IWGT)

Environmental and Molecular Mutagenesis, EarlyView.
Abstract Exposure levels without appreciable human health risk may be determined by dividing a point of departure on a dose–response curve (e.g., benchmark dose) by a composite adjustment factor (AF). An “effect severity” AF (ESAF) is employed in some regulatory contexts.
Barbara L. Parsons, Marc A. Beal, Kerry L. Dearfield, George R. Douglas, Min Gi, B. Bhaskar Gollapudi, Robert H. Heflich, Katsuyoshi Horibata, Michelle Kenyon, Alexandra S. Long, David P. Lovell, Anthony M. Lynch, Meagan B. Myers, Stefan Pfuhler, Alisa Vespa, Andreas Zeller, George E. Johnson, Paul A. White   +17 more
wiley   +1 more source

Oral Clefts with Associated Anomalies: Findings in the Hungarian Congenital Abnormality Registry [PDF]

, 2005
BACKGROUND: Over the years, great efforts have been made to record the frequency of orofacial clefts in different populations. However, very few studies were able to account for the etiological and phenotypic heterogeneity of these conditions. Thus, data
Czeizel, Andrew E., Sárközi, Andrea, Wyszynski, Diego F   +2 more
core   +3 more sources

Omphalocele and patent omphalomesenteric duct: A case report

Journal of Pediatric Surgery Case Reports
Introduction: The omphalomesenteric duct (OMD) is an embryonic structure that connects the yolk sac to the midgut. Under normal circumstances, it closes and self absorbes before birth.
Wassie Almaw Yigzaw, Abebe Tsegaye Danole, Abay Gosaye Wondimu   +2 more
doaj   +1 more source

Developmental outcomes after soybean oil vs mixed‐oil intravenous lipid emulsions in neonates: A secondary analysis of a clinical trial

Journal of Parenteral and Enteral Nutrition, EarlyView.
Abstract Background Fatty acids make up a significant portion of brain mass. The choice of lipid injectable emulsion alters a patient's fatty acid profile. In neonates with intestinal failure dependent on parenteral nutrition, this is particularly concerning given their rapid brain development. Methods We randomly assigned 24 infants to receive soy oil
Katie A. Huff, Charles Vanderpool
wiley   +1 more source

Complex ventral hernia secondary to giant omphalocele managed by preoperative pneumoperitoneum and botulinum toxin: A case report

Journal of Pediatric Surgery Case Reports, 2023
Introduction: Post-omphalocele ventral hernias pose significant challenges in pediatric surgery, often requiring multiple revision surgeries and carrying a high morbidity rate.
Mario Javier Peña García, Alejandro Alberto Peñarrieta Daher, Ivan Medina López, Sofía Brenes Guzmán, Cristian Zalles Vidal, Gustavo Teyssier Morales, Jaime Penchyna Grub, Jaime Nieto Zermeño, Ricardo Reynoso González   +8 more
doaj   +1 more source

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, Andrew M. George, Tom Lapidus, Cassandra Ligh, Suzanne P. MacFarland, Jennifer M. Kalish   +5 more
wiley   +1 more source