- This article provides an overview of chromosomal abnormalities associated with omphalocele and a comprehensive review of associated full aneuploidy such as trisomy 18, trisomy 13, triploidy, trisom...了解详细信息：This article provides an overview of chromosomal abnormalities associated with omphalocele and a comprehensive review of associated full aneuploidy such as trisomy 18, trisomy 13, triploidy, trisom...www.sciencedirect.com/science/article/pii/S102845…
It is a protrusion of the abdominal contents covered with peritoneum through the base of the umbilical cord. Omphalocele can be isolated but is more frequently associated with other congenital anomalies and syndromes such as Beckwith-Wiedemann syndrome and trisomies 13, 18, and 21.
www.ncbi.nlm.nih.gov/books/NBK519010/As the defect is observed in the Congolese fetuses or newborn babies, the purpose of this review is to clarify the main genetic risk factors associated with the omphalocele. This review is imaged by three omphalocele cases originated from Congo and France (Figs. 1 and 2 ).
jmhg.springeropen.com/articles/10.1186/s43042-0…Omphalocele (uhm-fa-lo-seal) is a birth defect of the abdominal (belly) wall. Surgery is needed to address the condition, putting any organs back into the belly and closing the opening. Researchers estimate that about 1 in every 4,000 babies is born with omphalocele in the United States.
www.cdc.gov/birth-defects/about/omphalocele.htmlMultiple genetic and environmental factors likely play a part in determining the risk of developing this disorder. When an abdominal wall defect, most often omphalocele, is a feature of a genetic condition, it is inherited in the pattern of that condition.
medlineplus.gov/genetics/condition/abdominal-wall … Omphalocele - StatPearls - NCBI Bookshelf
- 已发布: 2023/05/23
- Authors: Tarik Zahouani, Magda D. Mendez
- 附属关系: Lincoln Medical and Mental Health Center, Lincol…
Omphalocele is a rare congenital abdominal wall defect with a reported prevalence of 3.38 per 10,000 pregnancies.[1] It is a protrusion of the abdominal contents covered with peritoneum through the base of the umbilical cord. Omphalocele can be isolated but is more frequently associated with other c...Omphalocele: a review of common genetic etiologies
在jmhg.springeropen.com上查看更多信息Embryologically, omphalocele is an embryopathy resulting from an error in a midline abdominal wall development in early embryonic development (ED). Indeed, the normal development of the primitive intestine allows at 6 weeks of ED a normal physiologic herniation of the primitive mid-gut after undergoing the 90 degrees co…- 作者: Henriette Poaty, Fanny Pelluard, Mama Sy Diallo, Irène Patricia Lucienne Ondima, Gwenaelle André, Ja...
- 预计阅读时间：9 分钟
- Publish Year: 2019
- 发布日期: 2019年12月27日
- bing.com/videos观看完整视频观看完整视频
Omphalocele | Birth Defects | CDC
2024年5月16日 · Omphalocele (uhm-fa-lo-seal) is a birth defect of the abdominal (belly) wall. Surgery is needed to address the condition, putting any organs back into the belly and closing …
Abdominal wall defect: MedlinePlus Genetics
Multiple genetic and environmental factors likely play a part in determining the risk of developing this disorder. When an abdominal wall defect, most often omphalocele, is a feature of a genetic condition, it is inherited in the pattern of …
Omphalocele - Children's Hospital of Philadelphia
Genetic anomalies commonly seen with omphaloceles include abnormalities of chromosome number, such as trisomy 18, or genetic syndromes such as Beckwith-Wiedemann syndrome. A small omphalocele contains only bowel.
Syndromes and disorders associated with omphalocele (III
Omphalocele can be associated with single gene disorders, neural tube defects, diaphragmatic defects, fetal valproate syndrome, and syndromes of unknown etiology. This article provides a …
- 其他用户还问了以下问题
Chromosomal Abnormalities Associated With Omphalocele
2007年3月1日 · Omphalocele is a prominent marker for chromosomal abnormalities. Perinatal identification of omphalocele should alert chromosomal abnormalities and familial unbalanced …
Omphalocele | Genetic Consultations in the Newborn - Oxford …
This chapter reviews background information about the incidence, risk factors, genetics, recurrence risk, and epidemiology of isolated and syndromic omphalocele. The distinct …
Omphalocele: a review of common genetic etiologies
2019年12月1日 · Data have shown that omphalocele with co-occurring genetic abnormality has worse prognosis than isolated omphalocele.
Congenital omphalocele - NIH Genetic Testing Registry (GTR) - NCBI
An omphalocele is an abdominal wall defect limited to an open umbilical ring, and is characterized by the herniation of membrane-covered internal organs into the open base of the umbilical cord.
- 某些结果已被删除
