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Pediatric basilar invagination: Unveiling a rare complication of inflammatory bowel disease unclassified

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Author
Slivková, Pavla
Jevič, Filip
Schmidtová, Barbora
Smetanová, Jana
Kynčl, MartinORCiD Profile - 0000-0001-6210-6351Scopus Profile - 6701395942
Jačisko, JakubORCiD Profile - 0000-0002-4403-8217Scopus Profile - 57216993577
Kobesová, AlenaORCiD Profile - 0000-0002-7836-4723Scopus Profile - 6603255369

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Publication date
2024
Published in
PM and R
Volume / Issue
16 (7)
ISBN / ISSN
ISSN: 1934-1482
ISBN / ISSN
eISSN: 1934-1563
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  • 2. Faculty of Medicine

This publication has a published version with DOI 10.1002/pmrj.13203

Abstract
This case report details the presentation of an 8-year-old boy with atlantoaxial rotatory dislocation (AARD) and basilar invagination (BI), an exceedingly rare complication of inflammatory bowel disease unclassified (IBDU). Basilar invagination, an anomaly of the craniovertebral junction, results in the odontoid protruding into the foramen magnum. It may be associated with concurrent abnormalities such as atlantoaxial dislocation, Chiari malformation, atlas occipitalization, Klippel-Feil syndrome, atlanto-occipital hypoplasia, among others. To the best of our knowledge, this represents the first documented case reporting basilar invagination as a life-threatening complication of inflammatory bowel disease (IBD) in children.
Keywords
atlantoaxial rotatory dislocation, AARD, basilar invagination, BI, inflammatory bowel disease unclassified, IBDU, Case report
Permanent link
https://hdl.handle.net/20.500.14178/2558
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WOS:001247454300001
SCOPUS:2-s2.0-85196124046
PUBMED:38874265
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Full text of this result is licensed under: Creative Commons Uveďte původ 4.0 International

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