Literature DB >> 16788219

Multiple cysts in the liver autosomal dominant polycystic liver disease.

A A Karimbeg1, R J L F Loffeld.   

Abstract

A 45-year-old woman was admitted because of abdominal pain and a feeling of fullness. Ultrasound and CT scan of the abdomen showed a massively enlarged liver with hundreds of cysts and displacement of the right kidney. There were no cysts in the kidneys. Because several members of her family also had multiple cysts in the liver, the diagnosis of autosomal dominant polycystic liver disease (PCLD) was made. Genetic analysis demonstrated a protein kinase C substrate 80 K-H (PR KCSH) gene mutation (1338-2A>G) and confirmed the clinical diagnosis. A brief review of the genetics and possible treatments is given.

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Year:  2006        PMID: 16788219

Source DB:  PubMed          Journal:  Neth J Med        ISSN: 0300-2977            Impact factor:   1.422


  2 in total

1.  Cysts of PRKCSH mutated polycystic liver disease patients lack hepatocystin but express Sec63p.

Authors:  Esmé Waanders; Huib J E Croes; Cathy N Maass; René H M te Morsche; Hendrikus J A A van Geffen; J Han J M van Krieken; Jack A M Fransen; Joost P H Drenth
Journal:  Histochem Cell Biol       Date:  2008-01-26       Impact factor: 4.304

2.  Polycystic liver disease presenting with an exudative pleural effusion: a case report.

Authors:  Kerry Woolnough; Altav Palejwala; Simon Bramall
Journal:  J Med Case Rep       Date:  2012-04-13
  2 in total

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