A giant hypertrophy of C5 spinous process in Klippel-Feil syndrome; [Klippel-Feil sendromunda C5 spinöz proçesinin dev hipertrofisi]

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dc.contributor.authorMete M.
dc.contributor.authorÜnsal Ü.Ü.
dc.contributor.authorDuransoy Y.K.
dc.contributor.authorUmur A.Ş.
dc.contributor.authorSelçukİ M.
dc.date.accessioned2024-07-22T08:14:08Z
dc.date.available2024-07-22T08:14:08Z
dc.date.issued2015
dc.description.abstractCongenital cervical spinal anomalies are relatively common and can be seen in upper and lower cervical regions. However, hypertrophy of the lamina and spinous process of cervical vertebra is extremely rare. Here we reported an 11-year-old girl with unilateral hypertrophy of the lamina and spinous process of C5 vertebra coexistence with Klippel-Feil syndrome, occipitalization of atlas and atlantoaxial congenital fusion. Because of cosmetic anomaly patient underwent surgery and spinous process excised. To the best of our knowledge, this coexistence of congenital cervical bony anomalies in a child has not been reported previously in English literature. © 2015, Ege University Press. All rights reserved.
dc.identifier.issn13001817
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/16472
dc.language.isoEnglish
dc.publisherEge University Press
dc.subjectArticle
dc.subjectcase report
dc.subjectchild
dc.subjectcomputer assisted tomography
dc.subjectdisease association
dc.subjectfemale
dc.subjecthistology
dc.subjecthuman
dc.subjecthuman tissue
dc.subjecthypertrophy
dc.subjectKlippel Feil syndrome
dc.subjectnuclear magnetic resonance imaging
dc.subjectradiography
dc.subjectschool child
dc.subjectswelling
dc.subjectvertebra spinous process
dc.titleA giant hypertrophy of C5 spinous process in Klippel-Feil syndrome; [Klippel-Feil sendromunda C5 spinöz proçesinin dev hipertrofisi]
dc.typeArticle

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