Please use this identifier to cite or link to this item:
http://20.193.157.4:9595/xmlui/handle/123456789/1049Full metadata record
| DC Field | Value | Language |
|---|---|---|
| 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 |
| Appears in Collections: | Faculty of General Medicine | |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.