메뉴 건너뛰기




Volumn 48, Issue 7, 2009, Pages 749-750

Dyschromatosis universalis hereditaria in a young Nigerian female

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ANAMNESIS; ARTICLE; BODY DISTRIBUTION; CASE REPORT; CLINICAL FEATURE; DYSCHROMATOSIS UNIVERSALIS HEREDITARIA; EXTRACHROMOSOMAL INHERITANCE; FAMILY COUNSELING; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERPIGMENTATION; HYPOPIGMENTATION; MOTHER CHILD RELATION; NIGERIA; PHYSICAL EXAMINATION; PIGMENT DISORDER; SKIN BIOPSY; SKIN DEFECT; SKIN EXAMINATION;

EID: 67649199916     PISSN: 00119059     EISSN: 13654632     Source Type: Journal    
DOI: 10.1111/j.1365-4632.2009.03290.x     Document Type: Article
Times cited : (7)

References (12)
  • 3
    • 33646033001 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family
    • Bukhari IA, EL-Harith EA, Stuhrmann M. Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family. J Eur Acad Dermatol Venereol 2006; 20: 628-629.
    • (2006) J Eur Acad Dermatol Venereol , vol.20 , pp. 628-629
    • Bukhari, I.A.1    EL-Harith, E.A.2    Stuhrmann, M.3
  • 4
    • 0042242613 scopus 로고    scopus 로고
    • A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2
    • Xing Q, Wang M, Chen X, et al. A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2. Am J Hum Genet 2003; 73: 377-382.
    • (2003) Am J Hum Genet , vol.73 , pp. 377-382
    • Xing, Q.1    Wang, M.2    Chen, X.3
  • 6
    • 0000309721 scopus 로고
    • Genetical studies on skin diseases. VII. Dyschromatosis universalis hereditaria in five generations
    • Suenaga M. Genetical studies on skin diseases. VII. Dyschromatosis universalis hereditaria in five generations. Tohoku J Exp Med 1952; 55: 373-376.
    • (1952) Tohoku J Exp Med , vol.55 , pp. 373-376
    • Suenaga, M.1
  • 7
    • 0021595617 scopus 로고
    • Reticulate pigmentary disorders - A review
    • Griffiths WAD. Reticulate pigmentary disorders - a review. Clin Exp Dermatol 1984; 9: 439-450.
    • (1984) Clin Exp Dermatol , vol.9 , pp. 439-450
    • Griffiths, W.A.D.1
  • 9
    • 0036862123 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria: Report of a case and review of the literature
    • Al Hawsawi K, Al Aboud K, Ramesh V, et al. Dyschromatosis universalis hereditaria: Report of a case and review of the literature. Pediatr Dermatol 2002; 19: 223-226.
    • (2002) Pediatr Dermatol , vol.19 , pp. 223-226
    • Al Hawsawi, K.1    Al Aboud, K.2    Ramesh, V.3
  • 10
    • 0017737929 scopus 로고
    • Universal dyschromatosis with small stature and high tone deafness
    • Rycroft RJ, Calnan CD, Wells RS. Universal dyschromatosis with small stature and high tone deafness. Clin Exp Dermatol 1977; 2: 45-48.
    • (1977) Clin Exp Dermatol , vol.2 , pp. 45-48
    • Rycroft, R.J.1    Calnan, C.D.2    Wells, R.S.3
  • 11
    • 0026008752 scopus 로고
    • Dyschromatosis universalis hereditaria with epilepsy
    • Pavithran K. Dyschromatosis universalis hereditaria with epilepsy. Indian J Dermatol 1991; 57: 102-103.
    • (1991) Indian J Dermatol , vol.57 , pp. 102-103
    • Pavithran, K.1
  • 12
    • 0031085516 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria
    • Kim NS, Im S, Kim SC. Dyschromatosis universalis hereditaria. J Dermatol 1997; 24: 161-164.
    • (1997) J Dermatol , vol.24 , pp. 161-164
    • Kim, N.S.1    Im, S.2    Kim, S.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.