Co-occurrence of internal carotid artery agenesis with multicystic dysplastic kidney
| dc.contributor.author | Yilmaz Ovali G. | |
| dc.contributor.author | Tarhan S. | |
| dc.contributor.author | Bayindir P. | |
| dc.contributor.author | Polat M. | |
| dc.contributor.author | Akil I. | |
| dc.date.accessioned | 2025-04-10T11:16:02Z | |
| dc.date.available | 2025-04-10T11:16:02Z | |
| dc.date.issued | 2009 | |
| dc.description.abstract | Congenital 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-ID | 10.3906/sag-0706-11 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14701/51494 | |
| dc.title | Co-occurrence of internal carotid artery agenesis with multicystic dysplastic kidney | |
| dc.type | Article |