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2011, Number 3

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Med Sur 2011; 18 (3)

Enfermedad poliquística hepática asociada a enfermedad poliquística renal autosómica dominante

García GM, Sánchez-Zavala J, Mckinney NI, Corrales RB, Zavala GC, Brizuela AD, Herrera BH, Albores SJ, González CO

Language: Spanish
References: 11
Page: 132-135
PDF size: 215.78 Kb.


ABSTRACT

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited disorder; it is associated with mutations within genes that encode polycystins 1 and 2. These involve chromosomes 16 and 4 respectively. This entity develops extrarenal manifestations cystic and noncystic; ADPKD is more than a cystic disease affecting the kidneys and the liver. Extrarenal noncystic manifestations of ADPKD include vascular manifestations such as intracranial aneurysms. The polycystic liver disease can exist as isolated form or in association with ADPKD.


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