Dyschromatosis universalis hereditaria: a familial case with ultrastructural skin investigation

• المؤلفون الرئيسيون: Yi-Ying Chin (مؤلف), Gwo-Shing Chen (مؤلف), Stephen Chu-Sung Hu (مؤلف), Cheng-Che E. Lan (مؤلف)
• التنسيق: كتاب
• منشور في: Wolters Kluwer Medknow Publications, 2011-12-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Dyschromatosis universalis hereditaria (DUH) is a rare disease that is inherited both in autosomal dominant and autosomal recessive patterns. It is characterized by appearance of pinpoint to pea-sized hypo- and hyper-pigmented macules distributed in a reticulated pattern over the trunk and limbs wit...