Results 121 to 130 of about 401 (136)

Dermoscopic patterns of dyschromatosis universalis hereditaria with acral involvement

Clinical and Experimental Dermatology, 2023
Dyschromatosis universalis hereditaria is a rare inherited pigmentary disorder. It has a characteristic reticulate pigmentation involving the entire body, with acral sparing. The case is reported here for its unusual involvement of acral areas and reduced dermatoglyphs.
Ayanchetty Haripraba, Kaliaperumal Karthikeyan, Karthikeyan Kaliaperumal   +2 more
exaly   +3 more sources

Dyschromatosis universalis hereditaria (DUH)

CosmoDerma, 2022
Anmol Batra, Neirita Hazarika
openaire   +2 more sources

Dyschromatosis universalis hereditaria in a young Nigerian female

International Journal of Dermatology, 2009
AbstractDyschromatosis universalis hereditaria (DUH) is a clinically heterogeneous disorder that shows generalized mottled pigmentation. It occurs most commonly in Japanese persons, with sporadic reports from South Africa, India, and Iraq. Histopathology reveals a variable degree of pigmentary incontinence.
S M, Yusuf, M S, Mijinyawa, M B, Maiyaki, A Z, Mohammed   +3 more
exaly   +3 more sources

Dyschromatosis universalis hereditaria: two cases in a Chinese family

Clinical and Experimental Dermatology, 2005
Two cases of dyschromatosis universalis hereditaria (DUH) from a Chinese family are presented. Case 1 was a 62-year-old woman who had a generalized and progressive hyper- and hypopigmentation of the skin from the age of 8 years. Her brother had also developed a similar skin pigmentary defect from about the same age.
Gang Wang
exaly   +3 more sources

Dyschromatosis universalis hereditaria: a case report

International Journal of Dermatology, 2013
Shiva, Kumar, Okade, Rajendra, Harish, Prasad   +2 more
openaire   +3 more sources

An Interesting Case of Dyschromatosis Universalis Hereditaria

Journal of Pharmaceutical Negative Results, 2022
Nagapurapu Udaya, Manjumeena Dakshinamoorthy, Jayakar Thomas, K Naveen, U Dinesh, H Yadalla, S Pinninti, A Babu, C Naik, G Singh, T Rajashekar, R Okade, Al Hawsawi, K Al Aboud, K Ramesh, V Al Aboud, D, G Sethuraman, C Srinivas, M D'souza, D Thappa, L Smiles, U Nuber, S Tinschert, S Mundlos, I Hauber, C Zhang, D Li, J Zhang, X Chen, M Huang, S Archacki, Y Tian, W Ren, A Mei, Q Zhang, M Fang, Z Su, Y Yin, D Liu, Y Chen, X Cui, C Li, H Yang, Q Wang, J Wang, Y Deng, Sanjeev Gunjigavi, S Kumar, T Kumar, And, Ashwin Kulkarni, Manisha Sinha, Suresh Chandra Mondal, And Bhabotosh Makhal, K Thirupathi, Et Al, Achakanalli, And Santosh, Sadashivappa   +59 more
openaire   +3 more sources

Dyschromatosis Universalis Hereditaria: A Unique Disorder

Pediatric Dermatology, 2000
Gomathy Sethuraman, Devinder M. Thappa, null Vijaikumar, Jeevan Kumar, Sadagopan Srinivasan   +4 more
openaire   +2 more sources

Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family

Journal of the European Academy of Dermatology and Venereology, 2004
Abir Saraswat, Aj Kanwar
exaly   +2 more sources

Two Taiwanese siblings with dyschromatosis universalis hereditaria

Clinical and Experimental Dermatology, 2009
Two Taiwanese siblings presented with clinical and histological findings of dyschromatosis universalis hereditaria, which is an uncommon hereditary skin disease. A 26-year-old Taiwanese man had developed diffuse hyperpigmentation with hypopigmented spots over his whole body from the age of 4 years.
C Y, Wu, W H, Huang
openaire   +2 more sources

Dyschromatosis universalis hereditaria

Der Hautarzt, 2003
I. Elser, A. S. Hassan, J. Rieker, T. Ruzicka, M. Megahed   +4 more
openaire   +1 more source