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Revista Médica del Uruguay

On-line version ISSN 1688-0390


TOBAL, Diego  and  NOBOA, Oscar. Poliquistosis renal autosómica dominante: necesidad de diagnóstico y tratamiento oportuno. Rev. Méd. Urug. [online]. 2014, vol.30, n.3, pp.184-192. ISSN 1688-0390.

Abstract Autosomal dominant polycystic disease is the most common hereditary renal disease. Significant progress is being made today in order to slow down its advance. According to current evidence, early diagnosis and treatment of high blood pressure, cardiovascular risk factors, and kidney and extra-kidney complications are advisable. All kidney-prevention measures need to be applied to prevent the chronic kidney disease from advancing, and, if necessary, access to all techniques that replace kidney function are to be offered in an articulated manner, including kidney transplant. In spite of there being no evidence of an ideal medication for high bloodpressure, using inhibitors of the angiotensin converting enzyme and/or angiotensin II receptor antagonists appears to be advisable.


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