Copyright
©The Author(s) 2025.
World J Clin Cases. Nov 6, 2025; 13(31): 110620
Published online Nov 6, 2025. doi: 10.12998/wjcc.v13.i31.110620
Published online Nov 6, 2025. doi: 10.12998/wjcc.v13.i31.110620
Figure 1 Facial appearance of the patient diagnosed with dyschromatosis universalis hereditaria, showing widespread reticulated hyperpigmented macules predominantly on the forehead, cheeks, and nose.
Figure 2 Hyperpigmented macules distributed over the patient’s lower abdomen, groin, and bilateral lower limbs.
Figure 3 No dyschromatosis universalis hereditaria phenotype was observed in the baby.
- Citation: Wang XL, Zou T, Wu YC, Weng YY, Yao Q, Sun WW. Preventing transmission of dyschromatosis universalis hereditaria through preimplantation genetic testing: A case report. World J Clin Cases 2025; 13(31): 110620
- URL: https://www.wjgnet.com/2307-8960/full/v13/i31/110620.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v13.i31.110620
