Neonatal Dubin–Johnson syndrome: biochemical parameters, characteristics, and genetic variants study

Author:

Fu Haiyan,Zhao Ruiqin,Jia Xiaoyun,Li Xiaolei,Li Guigui,Yin Chunlan

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference26 articles.

1. Dubin, I. N. & Johnson, F. B. Chronic idiopathic jaundice with unidentified pigment in liver cells-a new clinicopathologic entity with a report of 12 cases. Medicine 33, 155–197 (1954).

2. Shani, M., Seligsohn, U., Gilon, E., Sheba, C. & Adam, A. Dubin-Johnson syndrome in Israel. I. Clinical, laboratory, and genetic aspects of 101 cases. Q. J. Med. 39, 549–567 (1970).

3. Memon, N., Weinberger, B. I., Hegyi, T. & Aleksunes, L. M. Inherited disorders of bilirubin clearance. Pediatr. Res. 79, 378–386 (2016).

4. Wu, L. et al. Mutation analysis of the ABCC2 gene in Chinese patients with Dubin-Johnson syndrome. Exp. Ther. Med. 16, 4201–4206 (2018).

5. Meng, L. L., Qiu, J. W., Lin, W. X. & Song, Y. Z. Clinical features and ABCC2 genotype of a baby with Dubin Johnson syndrome. Chin. J. Contemp. Pediatr. 21, 64–70 (2019).

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