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Case Reports
. 2017 Apr 20;130(8):1003-1005.
doi: 10.4103/0366-6999.204108.

Mixed Dubin-Gilbert Syndrome: A Compound Heterozygous Phenotype of Two Novel Variants in ABCC2 Gene

Jun Jiang  1 , Hua-Gui Wang  1 , Wei-Li Wu  1 , Xiang-Xin Peng  2
Affiliations
Case Reports

Mixed Dubin-Gilbert Syndrome: A Compound Heterozygous Phenotype of Two Novel Variants in ABCC2 Gene

Jun Jiang et al. Chin Med J (Engl). .
No abstract available

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Conflict of interest statement

There are no conflicts of interest.

Figures

Figure 1
Figure 1
The pigment shares some of its physicochemical properties with PAS-positive lipofuscin and melanin (arrow; D-PAS staining, original magnification × 400) (a). Increased amount of a coarsely granular brown pigment in liver cells (arrow; Schmorl staining, original magnification × 400) (b). DNA sequencing shows the UGT1A1 and ABCC2 gene mutations in the patient and her parents (arrows) (c). PAS: Periodic acid Schiff.
See this image and copyright information in PMC

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