Revisión y puesta al día en profundidad | 07 MAR 16

Enfermedad poliquística renal autosómica dominante del riñón

Es la enfermedad renal hereditaria más común con variada gravedad y extensión de las complicaciones extrarrenales.
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33 Chapman AB, Johnson AM, Rainguet S, Hossack K, Gabow P, Schrier RW. Left ventricular hypertrophy in autosomal dominant polycystic kidney disease. J Am Soc Nephrol  1997;8:1292-7.9259356.
34 Perrone RD, Abebe KZ, Schrier RW, et al. HALT PKD Study Group. Cardiac magnetic resonance assessment of left ventricular mass in autosomal dominant polycystic kidney disease. Clin J Am Soc Nephrol 2011;6:2508-15. doi:10.2215/CJN.04610511. 21903983.
35 Almeida EA, Oliveira EI, Lopes JA, Almeida AG, Prata MM. Tissue Doppler imaging in the evaluation of left ventricular function in young adults with autosomal dominant polycystic kidney disease. Am J Kidney Dis 2006;47:587-92. doi:10.1053/j.ajkd.2005.12.023. 16564936.
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37 Qian Q, Hartman RP, King BF, Torres VE. Increased occurrence of pericardial effusion in patients with autosomal dominant polycystic kidney disease. Clin J Am Soc Nephrol 2007;2:1223-7. doi:10.2215/CJN.01920507. 17928471.
38 Irazabal MV, Huston J 3rd, , Kubly V, et al. Extended follow-up of unruptured intracranial aneurysms detected by presymptomatic screening in patients with autosomal dominant polycystic kidney disease. Clin J Am Soc Nephrol 2011;6:1274-85. doi:10.2215/CJN.09731110. 21551026.
39 Xu HW, Yu SQ, Mei CL, Li MH. Screening for intracranial aneurysm in 355 patients with autosomal-dominant polycystic kidney disease. Stroke 2011;42:204-6. doi:10.1161/ STROKEAHA.110.578740. 21164130.
40 Pirson Y, Chauveau D, Torres V. Management of cerebral aneurysms in autosomal dominant polycystic kidney disease. J Am Soc Nephrol 2002;13:269-76.11752048.
41 Chapman JR, Hilson AJ. Polycystic kidneys and abdominal aortic aneurysms. Lancet 1980;1:646-7. doi:10.1016/S0140-6736(80)91135-6. 6102642. 
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48 Persu A, Duyme M, Pirson Y, et al. Comparison between siblings and twins supports a role for modifier genes in ADPKD.Kidney Int 2004;66:2132-6. doi:10.1111/j.1523-1755. 2004.66003.x. 15569302.
49 Simms RJ, Thong KM, Dworschak GC, Ong AC. Increased psychosocial risk, depression and reduced quality of life living with autosomal dominant polycystic kidney disease. Nephrol Dial Transplant 2015;gfv299. doi:10.1093/ndt/gfv299. 26268712.
50 Suwabe T, Ubara Y, Mise K, et al. Quality of life of patients with ADPKD-Toranomon PKD QOL study: cross-sectional study. BMC Nephrol 2013;14:179. doi:10.1186/1471-2369-14-179. 23978051.
51 Tong A, Rangan GK, Ruospo M, et al. A painful inheritance-patient perspectives on living with polycystic kidney disease: thematic synthesis of qualitative research. Nephrol Dial Transplant 2015;30:790-800. doi:10.1093/ndt/gfv010. 25637642.
52 Pei Y, Obaji J, Dupuis A, et al. Unified criteria for ultrasonographic diagnosis of ADPKD. J Am Soc Nephrol 2009;20:205-12. doi:10.1681/ASN.2008050507. 18945943.
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70 Grantham JJ, Chapman AB, Torres VE. Volume progression in autosomal dominant polycystic kidney disease: the major factor determining clinical outcomes. Clin J Am Soc Nephrol 2006;1:148-57. doi:10.2215/CJN.00330705. 17699202.
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