The co-occurrence of Chiari type 1 malformation with syringomyelia and total situs inversus

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dc.authoridAkdemir, Gokhan/0000-0002-1852-9442
dc.authoridDUMAN, Taskin/0000-0002-6552-4193
dc.contributor.authorSerarslan, Yurdal
dc.contributor.authorMelek, Ismet M.
dc.contributor.authorDuman, Taskin
dc.contributor.authorEraslan, Turali
dc.contributor.authorAkdemir, Goekhan
dc.contributor.authorYalcin, Fatih
dc.date.accessioned2024-09-18T20:59:14Z
dc.date.available2024-09-18T20:59:14Z
dc.date.issued2007
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractBackground: Total situs inversus (TSI) is a rare congenital anomaly that often occurs concomitantly with other disorders. TSI is the complete left-to-right inversion of the thoracic and abdominal organs. It develops due to an abnormal rotation of the cardiac tube during embryogenesis, the mechanism of which is of unknown mechanism. Syringomyelia (SM) is an uncommon disease of the spinal cord and is known as the occurrence of a cystic space in the middle of the spinal cord. SM occurs due to spinal cord injury, a primary tumor of the spinal cord, or an extramedullary lesion at the foramen magnum such as a Chiari type I malformation (CMI). In the literature there has been reported association of CMI and SM (CMI/SM) with known genetic syndromes. Case Report: We report a 33-year-old female with CMI/SM coexisting with TSI. Our patient presented with pain in the neck, arm, and upper back. She had no trsuma history. There was dysesthesia in the cervical-2 dermatomes. Radiological tools revealed that CMI/SM with TSI accompanied by no other abnormality. Conclusions: It can be suggested that the existence of this case indicates that genetic factors rnay influence the pathogenesis of some CMI/SM cases.en_US
dc.identifier.endpageCS113en_US
dc.identifier.issn1643-3750
dc.identifier.issue9en_US
dc.identifier.pmid17767123en_US
dc.identifier.scopus2-s2.0-34548672877en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpageCS110en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12483/12473
dc.identifier.volume13en_US
dc.identifier.wosWOS:000249684300012en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherInt Scientific Literature, Incen_US
dc.relation.ispartofMedical Science Monitoren_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectsyringomyeliaen_US
dc.subjecttotal situs inversusen_US
dc.subjectChiari type 1 malformationen_US
dc.titleThe co-occurrence of Chiari type 1 malformation with syringomyelia and total situs inversusen_US
dc.typeArticleen_US

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