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Partial 13 monosomy with corpus callosum agenesis and other congenital abnormalities – a case report

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dc.contributor.author Budeanu, Razvan-Gabriel
dc.contributor.author Jugariu, Anamaria-Romina
dc.contributor.author Katona, Timea
dc.contributor.author Băetu, Alexandru-Emil
dc.contributor.author Miron, Andreea-Iuliana
dc.date.accessioned 2020-07-03T12:33:14Z
dc.date.available 2020-07-03T12:33:14Z
dc.date.issued 2018
dc.identifier.citation BUDEANU, Razvan-Gabriel, JUGARIU, Anamaria-Romina, KATONA, Timea, BĂETU, Alexandru-Emil, MIRON, Andreea-Iuliana. Partial 13 monosomy with corpus callosum agenesis and other congenital abnormalities – a case report. In: MedEspera: the 7th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2018, p. 35-36. en_US
dc.identifier.uri https://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/10889
dc.description University of Medicine and Pharmacy of Targu Mures, Romania en_US
dc.description.abstract Background. The corpus callosum comprises the largest tract of nerve fibres in the human brain. It is developed from the telencephalon starting in the 11th week of foetal life. Partial or complete agenesis of the corpus callosum is a rare developmental anomaly of unknown cause. A case of corpus callosum agenesis is described. en_US
dc.language.iso en en_US
dc.publisher MedEspera en_US
dc.subject congenital malformations en_US
dc.subject genetic syndrome en_US
dc.subject corpus callosum agenesis en_US
dc.title Partial 13 monosomy with corpus callosum agenesis and other congenital abnormalities – a case report en_US
dc.type Article en_US


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  • MedEspera 2018
    The 7th International Medical Congress for Students and Young Doctors, May 3-5, 2018

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