DSpace Repository

Semilobarholoprosencephaly – A Dreading Congenital Anomaly.

Show simple item record

dc.contributor.author Bhushita B Lakhkar, Bhushan N Lakhkar, Bhavana B Lakhkar.
dc.date.accessioned 2019-11-25T05:42:59Z
dc.date.available 2019-11-25T05:42:59Z
dc.date.issued 2017-06
dc.identifier.uri http://hdl.handle.net/123456789/1361
dc.description.abstract Holoprosencephaly (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.iso en en_US
dc.publisher BLDE (Deemed to be University) en_US
dc.subject Corpus callosal agenesis, Failure of midline cleavage, Fused basal ganglia en_US
dc.title Semilobarholoprosencephaly – A Dreading Congenital Anomaly. en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account

Statistics