Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/1361
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dc.contributor.authorBhushita B Lakhkar, Bhushan N Lakhkar, Bhavana B Lakhkar.-
dc.date.accessioned2019-11-25T05:42:59Z-
dc.date.available2019-11-25T05:42:59Z-
dc.date.issued2017-06-
dc.identifier.urihttp://hdl.handle.net/123456789/1361-
dc.description.abstractHoloprosencephaly (HPE) is a group of structural abnormalities of brain that is an important cause of childhood mortality and morbidity. They usually occur due to impaired midline cleavage of embryonic forebrain i.e., failure of differentiation of the prosencephalon into the telecephalon and diencephalon. De Myer classified this anomaly ranging from alobar to semilobar and lobar type. It can be associated with microcephaly and midline facial anomalies. We present a case of semilobar holoprosencephaly with corpus callosal agenesis.en_US
dc.language.isoenen_US
dc.publisherBLDE (Deemed to be University)en_US
dc.subjectCorpus callosal agenesis, Failure of midline cleavage, Fused basal gangliaen_US
dc.titleSemilobarholoprosencephaly – A Dreading Congenital Anomaly.en_US
dc.typeArticleen_US
Appears in Collections:Faculty of Radiology

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