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Órgano Oficial del Instituto Nacional de Pediatría

2016, Number 1

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Acta Pediatr Mex 2016; 37 (1)

Chronic liver disease and hepatic insufficiency in an infant with ductal plate malformation

Zárate-Mondragón F, López-Corella E

Language: Spanish
References: 15
Page: 38-46
PDF size: 832.28 Kb.


Text Extraction

No abstract.


REFERENCES

  1. Ridaura Sanz C. Malformaciones congénitas de las vías biliares. En Uribe M. (Ed) MEDICINA INTERNA. 2ª Edición. Editorial Médica Panamericana. Buenos Aires. 1995.

  2. Desmet VJ. Ludwig symposium on biliary disorders--part I. Pathogenesis of ductal plate abnormalities. Mayo Clin Proc 1998;73:80-89.

  3. Escartín, P. Patología de la placa ductal. Gastroenterol Hepatol 1998;21:492-497.

  4. Desmet VJ. Congenital disease of intrahepatic bile ducts: variations on the theme “ductal plate malformation”. Hepatology 1992;16:1069-1083.

  5. Gunay-Aygun M. Liver and kidney disease in ciliopathies. Am J Med Genet C Semin Med Genet 2009;151C:296-306.

  6. Cnossen WR, Drenth JP. Polycystic liver disease: an overview of pathogenesis, clinical manifestations and management. Orphanet Journal of Rare Diseases. 2014;9:69. doi:10.1186/1750-1172-9-69.

  7. Gevers, TJ, Drenth, JP. Diagnosis and management of polycystic liver disease. Nat Rev Gastroenterol Hepatol 2013;10:101–8. doi: 10.1038/nrgastro.2012.254.

  8. Shorbagi A, Bayraktar Y. Experience of a single center with congenital hepatic fibrosis: A review of the literature. World J Gastroenterol 2010;16:683-90.

  9. Raynaud P, Tate J, Callens C, Cordi S, Vandersmissen P, et al. A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesis. Hepatology 2011;53:1959-66. doi: 10.1002/hep.24292.

  10. Rock N, McLin V. Liver involvement in children with ciliopathies. Clin Res Hepatol Gastroenterol 2014;38:407-14. doi: 10.1016/j.clinre.2014.04.001.

  11. Turkbey B, Ocak I, Daryanani K, Font-Montgomery E, Lukose L, Bryant J, Tuchman M, et al. Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF). Pediatr Radiol 2009;39:100–11.

  12. Desmet VJ. The Amazing Universe of Hepatic Microstructure. Hepatology 2009;50:333-44.

  13. Desmet V. Pathogenesis of ductal plate malformation. J Gastroenterol Hepatol 2004;19:356-60.

  14. Telega G, Cronin D, Avner E. New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney–liver complications. Pediatr Transplantation 2013;17:328–35.

  15. Jonas M, Pérez-Atayde A. Fibrocystic liver disease Capitulo 39. En: Suchy FJ, Sokol RJ, Balistreri WF. Liver disease in children. Edit. Cambridge University Press, Tercera edición, 2007.




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