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Boletín Médico del Hospital Infantil de México

2009, Number 2

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Bol Med Hosp Infant Mex 2009; 66 (2)

Alagille syndrome: A cause of intrahepatic cholestasis in childhood

Vázquez-Frias R, Worona-Dibner L, Cabrera-Muñoz ML, Sadowinski-Pine S

Language: Spanish
References: 24
Page: 178-188
PDF size: 1200.91 Kb.


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REFERENCES

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  3. Bezerra JA. Biliary atresia. En: Walkers, editor. Pediatric gastrointestinal disease. Approach to neonatal cholestasis. 5a ed. BC Decker Inc.; 2008. p. 817-29.

  4. Screiber RA, Kleinman RE. Biliary atresia. J Pediatr Gastroenterol Nutr. 2002: 35: S11-6.

  5. Karrer FM, Price MR, Bensard DD, Sokol RJ, Narkewicz MR, Smith DJ, et al. Long-term results with the Kasai operation for biliary atresia. Arch Surg. 1996; 131: 493-6.

  6. Balistreri WF. Intrahepatic cholestasis. J Pediatr Gastroenterol Nutr. 2002; 35: S17-23.

  7. Emerick KM, Rand EB, Goldmuntz E, Krantz ID, Spinner NB, Piccoli DA. Features of Alagille syndrome in 92 patients: Frequency and relation to prognosis. Hepatology. 1999; 29: 822-9.

  8. Ruben E, Quiros-Tejeria RE, Ament ME, Heyman MB, Martin MG, Rosenthal P, et al. Variable morbidity in Alagille syndrome: A review of 43 cases. J Pediatr Gastroenterol Nutr. 1999; 29: 431-8.

  9. Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, et al. Mutations in the human jagged 1 gene are responsible for Alagille syndrome. Nat Genet. 1997; 16: 235-42.

  10. Li L, Krantz ID, Deng Y, Genin A, Banta AB, Collins CC, et al. Alagille syndrome is caused by mutations in human Jagged 1, which encodes a ligand for Notch 1. Nat Genet. 1997; 16: 243-51.

  11. McDanielli R, Warthen DM, Sánchez-Lara PA, Pai A, Krantz ID, Piccoli DA, et al. NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the Notch Signaling Pathway. Am J Hum Genet. 2006; 79: 169-73.

  12. Lemaigre FP. Notch signaling in bile duct development: New insights raise new questions. Hepatology. 2008; 358-60.

  13. Alagille D, Estrada A, Hadchouel M, Gautier M, Odievre M, Dommergues JP. Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic displasia): review of 80 cases. J Pediatr. 1987; 110: 195-200.

  14. Deprettere A, Portmann B, Mowat AP. Syndromic paucity of the intrahepatic bile ducts: Diagnostic difficulty: Severe morbidity throughout childhood. J Pediatr Gastroenterol Nutr. 1987; 6; 865-71.

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  17. Dahms BB, Petrelli M, Wyllie R, Henoch MS, Halpin TC, Morrison S, et al. Arteriohepatic dysplasia in infancy and childhood: A longitudinal study of six patients. Hepatology. 1982; 2: 350-8.

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  21. Hoffenberg EJ, Narkewicz MR, Sondheimer JM. Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy. J Pediatr. 1995; 127: 220-4.

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