Copyright
©The Author(s) 2020.
World J Clin Cases. May 26, 2020; 8(10): 2001-2008
Published online May 26, 2020. doi: 10.12998/wjcc.v8.i10.2001
Published online May 26, 2020. doi: 10.12998/wjcc.v8.i10.2001
Figure 1 Peripheral blood smear (× 1000).
Few spherocytic red cells (orange arrow) appear in the proband and his parents. Additionally, acanthocytes (blue arrow) are easily seen in the father, whose hereditary spherocytosis genetic mutation (ANK1 c.925A>G) is different from the proband (ANK1 c.1801-17G>A) and the mother (ANK1 c.1801-17G>A).
- Citation: Kang LL, Liu ZL, Zhang HD. Gilbert’s syndrome coexisting with hereditary spherocytosis might not be rare: Six case reports. World J Clin Cases 2020; 8(10): 2001-2008
- URL: https://www.wjgnet.com/2307-8960/full/v8/i10/2001.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v8.i10.2001