European Journal of Medical Case Reports will consider any original case report that adds new information to existing general medical knowledge, and original research relating to case reports in all medical disciplines.

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Thin corpus callosum as a diagnostic marker for hereditary spastic paraparesis due to mutations in the SPG11 gene: a case report


Authors
Archana Murugan
1. Department of Paediatric Neurology, Bristol Royal Hospital for Children, Upper Maudlin Street, Bristol, BS2 8AE, United Kingdom
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Andrew Ashok Mallick
1. Department of Paediatric Neurology, Bristol Royal Hospital for Children, Upper Maudlin Street, Bristol, BS2 8AE, United Kingdom
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Laraine Dibble
2. Department of Paediatrics, Torbay Hospital, Lowes Bridge, Torquay, TQ2 7AA, United Kingdom
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Mohamed Osman Eltahir Babiker
1. Department of Paediatric Neurology, Bristol Royal Hospital for Children, Upper Maudlin Street, Bristol, BS2 8AE, United Kingdom
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Correspondence to:
Archana Murugan. Archana Murugan, 1. Department of Paediatric Neurology, Bristol Royal Hospital for Children, Upper Maudlin Street, Bristol, BS2 8AE, United Kingdom; archanamurugan@gmail.com

Publication history
Received 26 May 2017
Accepted 27 Jun 2017
Published in print 22 Sep 2017



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ISSN : 2520-4998