Generalized dyspigmentation on the body

Clinical and Experimental Dermatology

Volumn 34, Issue 6, 2009, Pages 737-738

  Aliagaoglu, C ^a   Atasoy, M ^a   Yildirim, U ^b,e   Erdem, T ^c   Erdem, C ^d   Engin, R I ^c  

^a Department of Dermatology ^*  (Turkey)

^b DUZCE UNIVERSITY   (Turkey)

^c ATATURK UNIVERSITY   (Turkey)

^d ANKARA UNIVERSITY   (Turkey)

^e ATATÜRK UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

MELANIN;

ADULT; ANAMNESIS; ARTICLE; CASE REPORT; CLINICAL FEATURE; DYSCHROMATOSIS UNIVERSALIS HEREDITARIA; GENODERMATOSIS; HISTOPATHOLOGIC SKIN REACTION; HUMAN; HUMAN TISSUE; HYPERPIGMENTATION; MALE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SKIN BIOPSY;

DISEASE PROGRESSION; HUMANS; HYPERPIGMENTATION; HYPOPIGMENTATION; MALE; YOUNG ADULT;

EID: 68249157947     PISSN: 03076938     EISSN: 13652230     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2008.02918.x     Document Type: Article

References (4)

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2. Wang G, Li CY, Gao TW, Liu YF. Dyschromatosis universalis hereditaria: two cases in a Chinese family. Clin Exp Dermatol 2005 30 : 494 6.
3. Sethuraman G, Srinivas CR, D'Souza M et al. Dyschromatosis universalis hereditaria. Clin Exp Dermatol 2002 27 : 477 9.
4. Nuber UA, Tinschert S, Mundlos S, Hauber I. Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation. Am J Med Genet A 2004 15 : 261 6.