Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature
Author:
Affiliation:
1. Dermatology Unit, Department of Medicine, King Faisal Hospital, Taif, Saudi Arabia, and
2. Department of Dermatology, King Khalid University Hospital, Riyadh, Saudi Arabia
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1525-1470.2002.00225.x
Reference20 articles.
1. Dyschromatosis
2. Genetical Studies on Skin Diseases
3. Dyschromatosis universalis hereditaria: report of a case;Kao CH;J Formos Med Assoc,1991
4. Dyschromatosis universalis hereditaria;Sait MA;Indian J Dermatol Venereol Leprol,1985
5. Hereditary congenital hypopigmented and hyperpigmented macules
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