Sporadic Dyschromatosis Universalis Hereditaria: A Second Case Report From Iran

被引：2
|
作者：
Dogohar, Sasan [1 ]
Alirezaei, Pedram [1 ]
Basir, Hamidreza Ghasemi [2 ]
Jamshidi, Mohammad [1 ]
Etaee, Farshid [3 ]
机构：
[1] Hamadan Univ Med Sci, Psoriasis Res Ctr, Hamadan, Hamadan, Iran
[2] Hamadan Univ Med Sci, Dept Pathol, Hamadan, Hamadan, Iran
[3] Texas Tech Univ, Hlth Sci Ctr Amarillo, Internal Med, Amarillo, TX 79106 USA
来源：
CUREUS JOURNAL OF MEDICAL SCIENCE | 2021年 / 13卷 / 07期
关键词：
dyschromatosis universalis hereditaria; duh; dermatology case report; genetic disorders; pigmentary disorders;
D O I：
10.7759/cureus.16511
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Dyschromatosis universalis hereditaria (DUH) is a rare pigmentary genodermatosis mostly reported from Japan. IL is usually characterized by widespread hyper/hypopigmented macules all over the body. Here, we report the case of a patient from Iran who presented with disseminated hyper and hypopigmented lesions over the trunk, neck, and extremities since the age of eight. lb the best of our knowledge, to date, there has been only one reported case of DUH from Iran.
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页数：4
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