Arnold Chiari Malformation Type 1: A case report.

SS Devarmani., Sandip J Singh

dc.contributor.author	SS Devarmani., Sandip J Singh
dc.date.accessioned	2019-11-02T11:32:52Z
dc.date.available	2019-11-02T11:32:52Z
dc.date.issued	2017
dc.identifier.issn	23479507
dc.identifier.uri	http://hdl.handle.net/123456789/1049
dc.description.abstract	Arnold-Chiari malformation is a constellation of congenital anomalies related to the hindbrain and base of the brain. It consists of cerebellar tonsils herniation through the foramen magnum into the cervical spinal canal. Chiari malformation is a rare entity and its etiology is not clearly known but said to be genetic. We report a case of Arnold Chiari Malformation type 1 with holocord syrinx.	en_US
dc.language.iso	en	en_US
dc.publisher	BLDE(Deemed to be University)	en_US
dc.subject	Arnold, Chiari, Congenital malformation, Syringomyelia, Syrinx	en_US
dc.title	Arnold Chiari Malformation Type 1: A case report.	en_US
dc.type	Article	en_US