Co-occurrence of internal carotid artery agenesis with multicystic dysplastic kidney

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dc.contributor.authorYilmaz Ovali G.
dc.contributor.authorTarhan S.
dc.contributor.authorBayindir P.
dc.contributor.authorPolat M.
dc.contributor.authorAkil I.
dc.date.accessioned2024-07-22T08:21:33Z
dc.date.available2024-07-22T08:21:33Z
dc.date.issued2009
dc.description.abstractCongenital absence of Internal Carotid Artery (ICA) is a rare disorder. This anomaly may be an isolated entity or may be associated with other organ, or system anomalies (1). Multicystic Dysplastic Kidney (MCDK) is a congenital mal-development in which the renal cortex is replaced by numerous cysts of multiple sizes. Urologic and non-urologic anomalies may accompany MCDK (2). In this paper, we detail a case of congenital agenesis of ICA and the existence of MCDK. To our knowledge, this is the first of such a case to be reported regarding the co-occurrence of ICA agenesis and MCDK. © TÜBİTAK.
dc.identifier.DOI-ID10.3906/sag-0706-11
dc.identifier.issn13000144
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/18670
dc.language.isoEnglish
dc.rightsAll Open Access; Bronze Open Access
dc.subjectHydraulic structures
dc.subjectIndependent component analysis
dc.subjectAgenesis
dc.subjectCarotid canal
dc.subjectCo-occurrence
dc.subjectInternal carotid artery
dc.subjectRenal cortex
dc.subjectarticle
dc.subjectcarotid artery anomaly
dc.subjectcase report
dc.subjectclinical feature
dc.subjecthuman
dc.subjectinfant
dc.subjectinternal carotid artery agenesis
dc.subjectlaboratory test
dc.subjectmagnetic resonance angiography
dc.subjectmale
dc.subjectmulticystic dysplastic kidney
dc.subjectnuclear magnetic resonance imaging
dc.subjectphysical examination
dc.subjectHemodynamics
dc.titleCo-occurrence of internal carotid artery agenesis with multicystic dysplastic kidney
dc.typeArticle

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