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<article xlink="http://www.w3.org/1999/xlink" dtd-version="1.0" article-type="healthcare" lang="en"><front><journal-meta><journal-id journal-id-type="publisher">IJCRR</journal-id><journal-id journal-id-type="nlm-ta">I Journ Cur Res Re</journal-id><journal-title-group><journal-title>International Journal of Current Research and Review</journal-title><abbrev-journal-title abbrev-type="pubmed">I Journ Cur Res Re</abbrev-journal-title></journal-title-group><issn pub-type="ppub">2231-2196</issn><issn pub-type="opub">0975-5241</issn><publisher><publisher-name>Open Science Publishers LLP</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">70</article-id><article-id pub-id-type="doi"/><article-id pub-id-type="doi-url"/><article-categories><subj-group subj-group-type="heading"><subject>Healthcare</subject></subj-group></article-categories><title-group><article-title>A RARE CASE REPORT OF DANDY WALKER MALFORMATION WITH LISSENCEPHALY, PARTIAL CORPUS CALLOSAL AGENESIS AND HYDROCEPHALUS&#13;
</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Sangramsinh</surname><given-names>Bhagat</given-names></name></contrib><contrib contrib-type="author"><name><surname>Kedar</surname><given-names>Athawale</given-names></name></contrib><contrib contrib-type="author"><name><surname>Dilip</surname><given-names>Lakhkar</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><day>21</day><month>09</month><year>2013</year></pub-date><volume>04</volume><issue>01</issue><fpage>1</fpage><lpage>4</lpage><permissions><copyright-statement>This article is copyright of Popeye Publishing, 2009</copyright-statement><copyright-year>2009</copyright-year><license license-type="open-access" href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.</license-p></license></permissions><abstract><p>Dandy-Walker malformation is characterised by agenesis or hypoplasia of the cerebellar vermis, cystic dilatation of the fourth ventricle, and enlargement of the posterior fossa. Approximately 70- 90% of patients have hydrocephalus. Lissencephaly is characterised by absence (agyria) or incomplete development (pachygyria) of the gyri of the cerebral cortex, causing the brain__ampersandsign#39;s surface to appear unusually smooth. Our case demonstrates Dandy Walker malformation with partial corpus callosal agenesis, hydrocephalus and Lissencephaly.&#13;
</p></abstract><kwd-group><kwd>Dandy Walker malformation</kwd><kwd> Lissencephaly</kwd></kwd-group></article-meta></front></article>
