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