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Revista de Medicina de Laboratorio 00009 / http://dx.doi.org/10.20960/revmedlab.00009

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Casos Clínicos

Recién nacido con debut de ictericia neonatal no isoinmune. Sindrome de Crigler-Najjar

María José Ruiz Márquez, Rocío Cabra-Rodríguez, Gema María Varo Sánchez

Prepublicado: 2020-06-09

Publicado: 2020-06-19

VOLUMEN 1, NÚM. 1, enero-abril (2020), PAG. 25-28

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Palabras Clave: Ictericia, Síndrome Crigler-Najjar, Glucuronosiltransferasa, Fenobarbital.

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Bibliografía

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-Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura, Y, Matsui, K, et al. Genotype of UGT1A1 and phenotype correlation between Crigler–Najjar syndrome type II and Gilbert syndrome.J Gastroenterol Hepatol 2016; 31(2): 403-408. https://doi.org/10.1111/jgh.13071
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-Li W, Yang L, Zhou W, Zhou Y. A novel deletion with two pathogenic variants of UGT1A1 causing Crigler-Najjar syndrome in two unrelated Chinese. Clin Biochem 2019; 71:67-68. https://doi.org/10.1016/j.clinbiochem.2019.06.013
DOI: 10.1016/j.clinbiochem.2019.06.013

-Dhawan A, Lawlor MW, Mazariegos GV, McKiernan P, Squires JE, Strauss KA, et al. Disease burden of Crigler–Najjar syndrome: Systematic review and future perspectives. J Gastroenterol Hepatol 2019. https://doi.org/10.1111/jgh.14853
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