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Symptomatic autosomal dominant polycystic liver disease (ADPLD) without polycystic kidney disease (ADPKD) in two generations of a family

✍ Scribed by Deepika Laxmi Koya; Ellen W. Shaw

Book ID: 119394820
Publisher: Nature Publishing Group
Year: 2003
Tongue: English
Weight: 22 KB
Volume: 98
Category: Article
ISSN: 0002-9270
DOI: 10.1016/s0002-9270(03)01247-4

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## Background: Autosomal-dominant polycystic kidney disease (adpkd) is characterized by gradual renal enlargement and cyst growth prior to loss of renal function. standard radiographic imaging has not provided the resolution and accuracy necessary to detect small changes in renal volume or to relia