Abstract: The objective of this review was to discuss the pathogenesis of Polycystic kidney disease (PKD), as well as the diagnosis and treatments approaches, through reviewing the evidence based on this manner. Databases; PubMed, and Embase were computerized searched for relevant studies concerning the Polycystic kidney disease (PKD), published in English language until the end of 2016. more relevant articles were extracted through searching the literature included in references of selected studies. Autosomal dominant polycystic kidney disease (ADPKD) is a common, acquired condition for which there is presently no effective specific medical therapy, pathologic accumulation of fluid in epithelium lined cavities causing the damage of adjacent regular parenchyma. Acquired cystic diseases, consisting of the most prevalent form, ADPKD, kidney ultrasonography is commonly utilized for the medical diagnosis of ADPKD and age-dependent criteria have been specified for subjects at-risk of PKD1. The utility of the PKD1 ultrasound criteria in the center setting is uncertain considering that their efficiency qualities have not been specified for the milder PKD2 and the gene type for a lot of test topics is unknown.
Keywords: Polycystic kidney disease (PKD), Diagnosis, treatments approaches.
Title: Polycystic Kidney Disease, Pathogenesis, Diagnosis, Treatment: Review
Author: Mohammed aqeel Jaafari, Mousa Mohammed Hadi, Faisal Mohammed Ali Gasmi, Ali shaya kaabi, Ahmad Mosa Ali Faqeeh, Anas Mohammed Alnahari
International Journal of Healthcare Sciences
ISSN 2348-5728 (Online)
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