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Omphalocele: a review of common genetic etiologies
- Source :
- Egyptian Journal of Medical Human Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
- Publication Year :
- 2019
- Publisher :
- Springer Science and Business Media LLC, 2019.
-
Abstract
- Omphalocele is one of the most common congenital defects in the anterior abdominal wall. The malformation is associated with various pathologies especially with chromosomal disorders. The developmental defect is observed in Congolese hospitals, but risk factors are not well precised on the published case reports, which are more often focused on management. We aim in this paper to make a review on the condition, insisting on the risk factors of omphaloceles mainly of those of genetic origins.
- Subjects :
- lcsh:R5-920
Pediatrics
medicine.medical_specialty
030219 obstetrics & reproductive medicine
Omphalocele
lcsh:QH426-470
Developmental defect
business.industry
medicine.disease
Abdominal wall defect
Abdominal wall
lcsh:Genetics
03 medical and health sciences
0302 clinical medicine
medicine.anatomical_structure
Medicine public health
Etiology
medicine
Congenital malformation
030212 general & internal medicine
lcsh:Medicine (General)
business
Genetic disorders
Genetics (clinical)
Subjects
Details
- ISSN :
- 20902441
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- Egyptian Journal of Medical Human Genetics
- Accession number :
- edsair.doi.dedup.....417cc6641c816ab76b6cfb9c9c4a1c02
- Full Text :
- https://doi.org/10.1186/s43042-019-0040-3