Co-occurrence of internal carotid artery agenesiswith multicystic dysplastic kidney
| dc.contributor.author | Ovali, GY | |
| dc.contributor.author | Tarhan, S | |
| dc.contributor.author | Bayindir, P | |
| dc.contributor.author | Polat, M | |
| dc.contributor.author | Akil, I | |
| dc.date.accessioned | 2024-07-18T11:49:44Z | |
| dc.date.available | 2024-07-18T11:49:44Z | |
| 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. | |
| dc.identifier.issn | 1300-0144 | |
| dc.identifier.other | 1303-6165 | |
| dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/4260 | |
| dc.language.iso | English | |
| dc.publisher | Tubitak Scientific & Technological Research Council Turkey | |
| dc.subject | CONGENITAL HORNERS-SYNDROME | |
| dc.subject | HYPOPLASIA | |
| dc.title | Co-occurrence of internal carotid artery agenesiswith multicystic dysplastic kidney | |
| dc.type | Article |