Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1584
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dc.contributor.authorREGNO:BN0120003-
dc.date.accessioned2023-12-11T10:43:51Z-
dc.date.available2023-12-11T10:43:51Z-
dc.date.issued2023-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1584-
dc.description.abstractBACKGROUND: In developed nations, congenital abnormalities are now a significant contributor to prenatal and neonatal mortality, and in developing nations like India, they may soon play an even significant role. Despite antenatal diagnostic methods, foetal autopsies are still extremely important for foetal congenital malformations to be confirmed, identified, and for counselling parents regarding future pregnancies. The direct advantages of autopsy for parents go beyond reducing the likelihood of recurrence. In cases where autopsy cannot reach a final diagnosis, the preservation of foetal samples for potential genetic research in the future offers the possibility of an accurate diagnosis. OBJECTIVE: 1. To study the prevalence of congenital anomalies in fetuses subjected for perinatal autopsy. 2. To assess the clinical efficiency of autopsy in reaching the final diagnosisen_US
dc.language.isoen_USen_US
dc.publisherKLE Academy of Higher Education and Research, Belagavien_US
dc.subjectKEYWORDS: Perinatal autopsy, Congenital malformation, anomalies, MTHFR gene, Still born, Genetics.en_US
dc.titlePREVALENCE OF CONGENITAL ANOMALIES IN FETUSES SUBJECTED FOR AUTOPSY – A HOSPITAL BASED CROSS SECTIONAL STUDYen_US
dc.typeDissertationsen_US
Appears in Collections:Pathology

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