Liver disease in autosomal recessive polycystic kidney disease

Pediatric Transplantation

Volumn 9, Issue 5, 2005, Pages 634-639

  Shneider, Benjamin L ^a,b,c   Magid, Margret S ^c  

^a Recanati/Miller Transplantation Institute   (United States)

^b MOUNT SINAI MEDICAL CENTER   (United States)

^c MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

Biliary; Congenital hepatic fibrosis; Cyst; Portal hypertension; Transplantation

Indexed keywords

FIBROCYSTIN;

BILE DUCT; BILIARY TRACT DISEASE; BLOOD CELL COUNT; CHOLANGIOGRAPHY; CHOLANGITIS; CONFERENCE PAPER; ECHOGRAPHY; GENE EXPRESSION; HUMAN; KIDNEY POLYCYSTIC DISEASE; KIDNEY TRANSPLANTATION; LIVER DISEASE; MAGNETIC RESONANCE CHOLANGIOGRAPHY; MEDICAL DECISION MAKING; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PHYSICAL EXAMINATION; PORTAL HYPERTENSION;

BILIARY TRACT DISEASES; HUMANS; HYPERTENSION, PORTAL; LIVER DISEASES; LIVER TRANSPLANTATION; POLYCYSTIC KIDNEY, AUTOSOMAL RECESSIVE;

EID: 26244464232     PISSN: 13973142     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-3046.2005.00342.x     Document Type: Conference Paper

References (23)

1. GUAY-WOODFORD LM, DESMOND RA. Autosomal recessive polycystic kidney disease: The clinical experience in North America. Pediatrics 2003: 111: 1072-1080.
2. DAVIS ID, HO M, HUPERTZ V, AVNER ED. Survival of childhood polycystic kidney disease following renal transplantation: The impact of advanced hepatobiliary disease. Pediatr Transplant 2003: 7: 364-369.
3. ZERRES K, MUCHER G, BACHNER L, et al. Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen. Nat Genet 1994: 7: 429-432.
4. LAGER DJ, QIAN Q, BENGAL RJ, ISHIBASHI M, TORRES VE. The pck rat: A new model that resembles human autosomal dominant polycystic kidney and liver disease. Kidney Int 2001: 59: 126-136.
5. SANZEN T, HARADA K, YASOSHIMA M, KAWAMURA Y, ISHIBASHI M, NAKANUMA Y. Polycystic kidney rat is a novel animal model of Caroli's disease associated with congenital hepatic fibrosis. Am J Pathol 2001: 158: 1605-1612.
6. ONUCHIC LF, FURU L, NAGASAWA Y, et al. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats. Am J Hum Genet 2002: 70: 1305-1317.
7. WARD CJ, HOGAN MC, ROSSETTI S, et al. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein. Nat Genet 2002: 30: 259-269.
8. HARRIS PC, ROSSETTI S. Molecular genetics of autosomal recessive polycystic kidney disease. Mol Genet Metab 2004: 81: 75-85.
9. ZHANG MZ, MAI W, LI C, et al. PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells. Proc Natl Acad Sci USA 2004: 101: 2311-2316.
10. MASYUK TV, HUANG BQ, WARD CJ, et al. Defects in cholangiocyte fibrocystin expression and ciliary structure in the PCK rat. Gastroenterology 2003: 125: 1303-1310.
11. ONG AC, WHEATLEY DN. Polycystic kidney disease - the ciliary connection. Lancet 2003: 361: 774-776.
12. JORGENSEN MJ. The ductal plate malformation. Acta Pathol Microbiol Scand Suppl 1977: 1-87.
13. DESMET VJ. Ludwig symposium on biliary disorders - part I. Pathogenesis of ductal plate abnormalities. Mayo Clin Proc 1998: 73: 80-89.
14. SUMMERFIELD JA, NAGAFUCHI Y, SHERLOCK S, CADAFALCH J, SCHEUER PJ. Hepatobiliary fibropolycystic diseases. A clinical and histological review of 51 patients. J Hepatol 1986: 2: 141-156.
15. MCCARTHY L, BAGGENSTOSS A, LOGAN G. Congenital hepatic fibrosis. Gastroenterology 1965: 49: 27-31.
16. KHAN K, SCHWARZENBERG SJ, SHARP HL, MATAS AJ, CHAVERS BM. Morbidity from congenital hepatic fibrosis after renal transplantation for autosomal recessive polycystic kidney disease. Am J Transplant 2002: 2: 360-365.
17. ABOUCHACRA S, TOUMEH S, BOOBES Y, BERNIEH B, GORKA W. An atypical course of Caroli's disease in a renal transplant patient - case report and review of the literature. Clin Nephrol 2004: 61: 282-288.
18. CAPISONDA R, PHAN V, TRAUBUCI J, DANEMAN A, BALFE JW, GUAY-WOODFORD LM. Autosomal recessive polycystic kidney disease: Outcomes from a single-center experience. Pediatr Nephrol 2003: 18: 119-126.
19. NORTON KI, GLASS RB, KOGAN D, EMRE S, SCHWARTZ M, SHNEIDER BL. MR cholangiography in children and young adults with biliary disease. AJR Am J Roentgenol 1999: 172: 1239-1244.
20. SHNEIDER B. Portal hypertension. In: SUCHY F, SOKOL R, BALISTRERI W, eds. Liver Disease in Children. Philadelphia: Lippincott Williams & Wilkins, 2001: pp. 129-151.
21. SANTAMARIA F, SARNELLI P, CELENTANO L, et al. Noninvasive investigation of hepatopulmonary syndrome in children and adolescents with chronic cholestasis. Pediatr Pulmonol 2002: 33: 374-379.
22. BARBE T, LOSAY J, GRIMON G, et al. Pulmonary arteriovenous shunting in children with liver disease. J Pediatr 1995: 126: 571-579.
23. TSIMARATOS M, CLOAREC S, ROQUELAURE B, et al. Chronic renal failure and portal hypertension - is portosystemic shunt indicated? Pediatr Nephrol 2000: 14: 856-858.