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dc.contributor.authorOzcora, Gul Demet Kaya
dc.contributor.authorKumandas, Sefer
dc.contributor.authorSagiroglu, Ayse
dc.contributor.authorAcer, Niyazi
dc.contributor.authorDoganay, Selim
dc.contributor.authorYigit, Huseyin
dc.contributor.authorCanpolat, Mehmet
dc.contributor.authorPer, Huseyin
dc.contributor.authorGumus, Hakan
dc.date.accessioned2023-07-31T10:25:11Z
dc.date.available2023-07-31T10:25:11Z
dc.date.issued2022en_US
dc.identifier.citationOzcora, G. D. K., Kumandas, S., Sagiroglu, A., Acer, N., Doganay, S., Yigit, H., ... & Gumus, H. (2022). Evaluating the brainstem in children with breath-holding spells. Northern Clinics of Istanbul, 9(6), 610.en_US
dc.identifier.issn2148-4902
dc.identifier.urihttps://doi.org/10.14744/nci.2022.82085
dc.identifier.urihttps://hdl.handle.net/20.500.12294/3936
dc.description.abstractOBJECTIVE: Breath-holding spells (BHSs) are a non-epileptic paroxysmal phenomenon characterized by frequent apnea episodes, loss of consciousness, and changes in skin tone and postural tone triggered by negative stimuli of childhood. The pathophysiology of the disease remains unclear; autonomic dysregulation caused by delayed myelination is believed to play a role. In this study, we aimed to evaluate the brainstems of children with BHS using diffusion tensor imaging (DTI) and investigate the etiology of this phenomenon. METHODS: The study group consisted of 16 children with a history of severe breath-holding episodes (accompanied by loss of consciousness and tonic contraction due to prolonged anoxic response) and 18 age-, gender-, and handedness-matched controls. All children underwent systemic, neurologic, and cardiologic evaluation, including complete blood count, blood biochemistry, serum iron and ferritin level, serum vitamin B12 level, electrocardiogram, and electroencephalograms. Magnetic resonance imaging was performed using a 1.5-Tesla Siemens Aera scanner (Siemens, Germany). RESULTS: Evaluation of brainstem (midbrain, pons, and medulla oblongata) volumes revealed no statistically significant differences between the BHS patient and control groups. In a voxel-wise analysis of DTI data, the BHS patient group had significantly lower fractional anisotropy (FA) values than the control group in the bilateral midbrain and medulla, right corticospinal tract, bilateral corpus callosum body and splenium, and left corpus callosum genu. In contrast, there were no significant differences in FA values in the pons, cerebellum, left corticospinal tract, and right corpus callosum genu. CONCLUSION: Based on our findings, we think that patients with BHS should be treated with an approach similar to other neurodevelopmental diseases and that this study may help elucidate the pathophysiology and establish the groundwork for future studies on its treatment. © 2022 by Istanbul Provincial Directorate of Health.en_US
dc.language.isoengen_US
dc.publisherKare Publishingen_US
dc.relation.ispartofNorthern Clinics of Istanbulen_US
dc.identifier.doi10.14744/nci.2022.82085en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBrainstemen_US
dc.subjectbreath-holdingen_US
dc.subjectchilden_US
dc.titleEvaluating the brainstem in children with breathholding spellsen_US
dc.typearticleen_US
dc.departmentTıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.authorid0000-0002-4155-7759en_US
dc.identifier.volume9en_US
dc.identifier.issue6en_US
dc.identifier.startpage610en_US
dc.identifier.endpage615en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.institutionauthorAcer, Niyazi
dc.authorscopusid14419755900en_US
dc.identifier.scopus2-s2.0-85164724550en_US


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