Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family [17]

Journal of the European Academy of Dermatology and Venereology

Volumn 20, Issue 5, 2006, Pages 628-629

  Bukhari, I A ^a   El Harith, E A ^b   Stuhrmann, M ^b  

^a IMAM ABDULRAHMAN BIN FAISAL UNIVERSITY   (Saudi Arabia)

^b HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHILD; CHILD DEVELOPMENT; CHROMOSOME 1Q; CHROMOSOME 6Q; DEPIGMENTATION; DYSCHROMATOSIS UNIVERSALIS HEREDITARIA; FAMILY STUDY; FEMALE; FOLLOW UP; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; LETTER; MALE; ONSET AGE; PRIORITY JOURNAL; SAUDI ARABIA; SKIN BIOPSY;

ADULT; CHILD; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; MALE; PIGMENTATION DISORDERS; SKIN DISEASES, GENETIC;

EID: 33646033001     PISSN: 09269959     EISSN: 14683083     Source Type: Journal    
DOI: 10.1111/j.1468-3083.2006.01522.x     Document Type: Letter

References (6)

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3. Zhang XJ, Gao M, Li M et al. Identification of a locus for dyschromatosis symmetrica hereditaria at 1q11-1q21. J Invest Dermatol 2003; 120: 776-780.
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