Autosomal dominant polycystic kidney disease
Diagnosis certain
Updates to Study Attributes
Findings
was changed:
There are innumerable cysts of varying sizes in the liver, and bilateral kidneys with little remaining normal renal parenchyma. No evidence of hemorrhagic cysts.
Updates to Case Attributes
Body
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This case shows an autosomal dominant polycystic kidney disease (ADPKD) with extra-renal manifestation (liver).
ADPKDADPKD is the most common hereditary renal disease andand is commonly associated with polycystic liver disease (75% of patients with ADPKD).
-<p>This case shows an<strong> autosomal dominant polycystic kidney disease (ADPKD) </strong>with extra-renal manifestation (liver).</p><p> ADPKD is the most common hereditary renal disease and is commonly associated with polycystic liver disease (75% of patients with ADPKD).</p>- +<p>This case shows an<strong> autosomal dominant polycystic kidney disease (ADPKD) </strong>with extra-renal manifestation (liver).</p><p>ADPKD is the most common hereditary renal disease and is commonly associated with polycystic liver disease (75% of patients with ADPKD).</p>
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