| Literature DB >> 21983864 |
Veronica Saletti1, Silvia Esposito, Manuela Frittoli, Laura Grazia Valentini, Luisa Chiapparini, Sara Bulgheroni, Daria Riva.
Abstract
The clinical features of Chiari I Malformation (CIM) may be related to the compression of dural and/or neural structures at the craniocervical junction or to the associated syringomyelia. Additionally, patients may exhibit symptoms and signs of associated disorders. CIM is a heterogeneous and multifactorial disorder including congenital and acquired forms; it can also be found as an isolated malformation or in association with many clinical conditions. We analyse the clinical features in a series of 65 children with CIM, focusing on the high frequency of associated clinical disorders. We emphasise the importance of a careful clinical and neurological assessment for a proper diagnosis and a correct management of these patients.Entities:
Mesh:
Year: 2011 PMID: 21983864 DOI: 10.1007/s10072-011-0744-8
Source DB: PubMed Journal: Neurol Sci ISSN: 1590-1874 Impact factor: 3.307