dc.contributorUniversidade Estadual Paulista (UNESP)
dc.contributorMedicine School of São José do Rio Preto
dc.date.accessioned2022-04-29T08:00:15Z
dc.date.accessioned2022-12-20T02:37:02Z
dc.date.available2022-04-29T08:00:15Z
dc.date.available2022-12-20T02:37:02Z
dc.date.created2022-04-29T08:00:15Z
dc.date.issued2013-01-01
dc.identifierJournal of Pediatric Genetics, v. 2, n. 2, p. 85-90, 2013.
dc.identifier2146-460X
dc.identifier2146-4596
dc.identifierhttp://hdl.handle.net/11449/228288
dc.identifier10.3233/PGE-13052
dc.identifier2-s2.0-85013578705
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5408423
dc.description.abstractBirth defects (BDs) or congenital anomalies include all structural and functional alterations in embryonic or fetal development resulting from genetic, environmental or unknown causes, which result in physical and/or mental impairment. BDs occur in about 3% of newborn babies and in most cases of pregnancy loss. BDs are a very complex and heterogeneous group of single or multiple changes that, in most cases, are of unknown etiology. Among the risk factors are advanced maternal and paternal ages, parental consanguinity, teratogenic agents such as infectious agents and drugs, and poor nutrition, in particular folic acid deficiency. One of the consequences of these defects is the high death rate within the first year of life. Information on BDs is becoming increasingly more important throughout the world so that preventive measures can be taken. Knowledge of BDs enables the development of therapeutic and preventive strategies besides adequate genetic counseling. © 2013 - IOS Press and the authors.
dc.languageeng
dc.relationJournal of Pediatric Genetics
dc.sourceScopus
dc.subjectChromosomal abnormalities
dc.subjectCongenital anomalies
dc.subjectCongenital malformation
dc.titleBirth defects: Risk factors and consequences
dc.typeArtículos de revistas


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