Radio‑Diagnostic Evaluation of Adult Polycystic Disease of  the Kidneys and Liver in a 53‑Year‑Old Homemaker – A Case  Report and Review of the Literature

AYARA, Charles O

dc.contributor.author	AYARA, Charles O
dc.date.accessioned	2024-04-24T09:03:08Z
dc.date.available	2024-04-24T09:03:08Z
dc.date.issued	2023-08-18
dc.identifier.citation	Ayara, et al.: Radio‑diagnostic evaluation of adult polycystic disease of the kidneys and liver in a 53‑year‑old homemaker	en_US
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/1008
dc.description.abstract	Autosomal dominant polycystic kidney disease (ADKPD) is the most common hereditary kidney disease and one of the most common causes of end‑stage kidney diseases, with approximately 30% of patients with ADKPD having polycystic liver in addition. A case of a 53‑year‑old homemaker who presented with marked abdominal swelling, distension, and respiratory distress, in whom ultrasonographic and computed tomographic features of multiple noncommunicating cystic lesions in the kidneys and the liver were demonstrated, was presented to emphasize the key role of medical imaging in the diagnosis of ADKPD. A review of the literature was also done.	en_US
dc.description.sponsorship	Self-sponsored	en_US
dc.publisher	Published by Wolters Kluwer - Medknow	en_US
dc.relation.ispartofseries	1 (2);
dc.subject	Adult polycystic kidney disease	en_US
dc.subject	, autosomal dominant	en_US
dc.subject	genes	en_US
dc.subject	hereditary disease	en_US
dc.title	Radio‑Diagnostic Evaluation of Adult Polycystic Disease of the Kidneys and Liver in a 53‑Year‑Old Homemaker – A Case Report and Review of the Literature	en_US
dc.type	Article	en_US