Literature DB >> 16677351

Predominant extrahepatic biliary disease in autosomal recessive polycystic kidney disease: a new association.

Beatrice Goilav1, Karen I Norton, Lisa M Satlin, Lisa Guay-Woodford, Frank Chen, Margret S Magid, Sukru Emre, Benjamin L Shneider.   

Abstract

Autosomal recessive polycystic kidney disease (ARPKD) is characterized by dilation of ectatic renal collecting ducts, intrahepatic biliary dysgenesis, and portal fibrosis. Portal hypertension and recurrent bacterial cholangitis can dominate the clinical picture in long-term survivors. Predominant extrahepatic bile duct disease was revealed in four patients who underwent magnetic resonance cholangiopancreatography. All four patients had portal hypertension, although liver biochemistries did not suggest biliary disease. In two of the patients, cholangitis was clinically ascribed to the bile duct disease. Western blot analysis of plasma membranes from normal rat extrahepatic bile duct and kidney revealed the presence of polyductin as a single approximately 440 kDa protein. Although the exact function of polyductin in the extrahepatic duct is unknown, it may have a role in the development and control of lumenal size. Clinical management of patients with ARPKD should include consideration of potential problems related to extrahepatic bile duct disease.

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Year:  2006        PMID: 16677351     DOI: 10.1111/j.1399-3046.2005.00456.x

Source DB:  PubMed          Journal:  Pediatr Transplant        ISSN: 1397-3142


  9 in total

Review 1.  Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease.

Authors:  Arvind Srinath; Benjamin L Shneider
Journal:  J Pediatr Gastroenterol Nutr       Date:  2012-05       Impact factor: 2.839

2.  Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference.

Authors:  Meral Gunay-Aygun; Ellis D Avner; Robert L Bacallao; Peter L Choyke; Joseph T Flynn; Gregory G Germino; Lisa Guay-Woodford; Peter Harris; Theo Heller; Julie Ingelfinger; Frederick Kaskel; Robert Kleta; Nicholas F LaRusso; Parvathi Mohan; Gregory J Pazour; Benjamin L Shneider; Vicente E Torres; Patricia Wilson; Colleen Zak; Jing Zhou; William A Gahl
Journal:  J Pediatr       Date:  2006-08       Impact factor: 4.406

Review 3.  Liver and kidney disease in ciliopathies.

Authors:  Meral Gunay-Aygun
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

4.  Characteristics of congenital hepatic fibrosis in a large cohort of patients with autosomal recessive polycystic kidney disease.

Authors:  Meral Gunay-Aygun; Esperanza Font-Montgomery; Linda Lukose; Maya Tuchman Gerstein; Katie Piwnica-Worms; Peter Choyke; Kailash T Daryanani; Baris Turkbey; Roxanne Fischer; Isa Bernardini; Murat Sincan; Xiongce Zhao; Netanya G Sandler; Annelys Roque; Daniel C Douek; Jennifer Graf; Marjan Huizing; Joy C Bryant; Parvathi Mohan; William A Gahl; Theo Heller
Journal:  Gastroenterology       Date:  2012-10-03       Impact factor: 22.682

Review 5.  Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

Authors:  Jayanthi Chandar; Jennifer Garcia; Lydia Jorge; Akin Tekin
Journal:  Pediatr Nephrol       Date:  2014-08-13       Impact factor: 3.714

6.  Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease.

Authors:  Meral Gunay-Aygun; Esperanza Font-Montgomery; Linda Lukose; Maya Tuchman; Jennifer Graf; Joy C Bryant; Robert Kleta; Angelica Garcia; Hailey Edwards; Katie Piwnica-Worms; David Adams; Isa Bernardini; Roxanne E Fischer; Donna Krasnewich; Neal Oden; Alex Ling; Zenaide Quezado; Colleen Zak; Kailash T Daryanani; Baris Turkbey; Peter Choyke; Lisa M Guay-Woodford; William A Gahl
Journal:  Clin J Am Soc Nephrol       Date:  2010-04-22       Impact factor: 8.237

7.  Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1.

Authors:  Anna-Rachel Gallagher; Ernie L Esquivel; Tiffany S Briere; Xin Tian; Michihiro Mitobe; Luis F Menezes; Glen S Markowitz; Dhanpat Jain; Luiz F Onuchic; Stefan Somlo
Journal:  Am J Pathol       Date:  2008-01-17       Impact factor: 4.307

Review 8.  Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF).

Authors:  Baris Turkbey; Iclal Ocak; Kailash Daryanani; Esperanza Font-Montgomery; Linda Lukose; Joy Bryant; Maya Tuchman; Parvathi Mohan; Theo Heller; William A Gahl; Peter L Choyke; Meral Gunay-Aygun
Journal:  Pediatr Radiol       Date:  2008-12-17

9.  MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome.

Authors:  Meral Gunay-Aygun; Melissa A Parisi; Dan Doherty; Maya Tuchman; Ekaterini Tsilou; David E Kleiner; Marjan Huizing; Baris Turkbey; Peter Choyke; Lisa Guay-Woodford; Theo Heller; Katarzyna Szymanska; Colin A Johnson; Ian Glass; William A Gahl
Journal:  J Pediatr       Date:  2009-06-21       Impact factor: 4.406

  9 in total

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