Congenital dysfibrinogenemia misdiagnosed and inappropriately treated as acute fatty liver in pregnancy: A case report and review of literature

doi:10.12998/wjcc.v10.i35.12996

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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Case Report

World J Clin Cases. Dec 16, 2022; 10(35): 12996-13005
Published online Dec 16, 2022. doi: 10.12998/wjcc.v10.i35.12996

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Figure 1 Pedigree. Affected II1 (proband) had congenital dysfibrinogenemia and carried the genetic mutation in the fibrinogen alpha chain gene (p.R350H). I1, I3, II1, and III1 carry the causative pathogenic gene.

Citation: Jia Y, Zhang XW, Wu YS, Wang QY, Yang SL. Congenital dysfibrinogenemia misdiagnosed and inappropriately treated as acute fatty liver in pregnancy: A case report and review of literature. World J Clin Cases 2022; 10(35): 12996-13005
URL: https://www.wjgnet.com/2307-8960/full/v10/i35/12996.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i35.12996

Jia Y, Zhang XW, Wu YS, Wang QY, Yang SL. Congenital dysfibrinogenemia misdiagnosed and inappropriately treated as acute fatty liver in pregnancy: A case report and review of literature. World J Clin Cases 2022; 10(35): 12996-13005 [PMID: 36569010 DOI: 10.12998/wjcc.v10.i35.12996]

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