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Volumn 17, Issue 2, 2011, Pages 2-

Dyschromatosis universalis hereditaria: A case report

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ALOPECIA; ARTICLE; ASYMPTOMATIC DISEASE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; DEPIGMENTATION; DYSCHROMATOSIS UNIVERSALIS HEREDITARIA; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERKERATOSIS; HYPERPIGMENTATION; HYPOPIGMENTATION; INDIAN; MALE; NAIL DYSTROPHY; PAPULE; PIGMENT DISORDER; SCHOOL CHILD; SKIN BIOPSY; SKIN EXAMINATION;

EID: 79953065223     PISSN: 10872108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (10)

References (7)
  • 2
    • 23044432575 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria: Two cases in a Chinese family
    • Sep; [PubMed]
    • Wang G, Li CY, Gao TW, Liu YF. Dyschromatosis universalis hereditaria: two cases in a Chinese family. Clin Exp Dermatol. 2005 Sep;30(5):494-6. [PubMed]
    • (2005) Clin Exp Dermatol. , vol.30 , Issue.5 , pp. 494-496
    • Wang, G.1    Li, C.Y.2    Gao, T.W.3    Liu, Y.F.4
  • 3
    • 33746869673 scopus 로고    scopus 로고
    • Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria
    • Jul-Aug; [PubMed]
    • Binitha MP, Thomas D, Asha LK. Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria. Indian J Dermatol Venereol Leprol. 2006 Jul-Aug;72(4):300-2. [PubMed]
    • (2006) Indian J Dermatol Venereol Leprol. , vol.72 , Issue.4 , pp. 300-302
    • Binitha, M.P.1    Thomas, D.2    Asha, L.K.3
  • 4
    • 0017737929 scopus 로고
    • Universal dyschromatosis, small stature and high-tone deafness
    • Mar; [PubMed]
    • Rycroft RJ, Calnan CD, Wells RS. Universal dyschromatosis, small stature and high-tone deafness. Clin Exp Dermatol. 1977 Mar;2(1):45-8. [PubMed]
    • (1977) Clin Exp Dermatol. , vol.2 , Issue.1 , pp. 45-48
    • Rycroft, R.J.1    Calnan, C.D.2    Wells, R.S.3
  • 5
    • 33646033001 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family
    • May; [PubMed]
    • 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 May;20(5):628-9. [PubMed]
    • (2006) J Eur Acad Dermatol Venereol. , vol.20 , Issue.5 , pp. 628-629
    • Bukhari, I.A.1    El-Harith, E.A.2    Stuhrmann, M.3
  • 6
    • 0036862123 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria: Report of a case and review of the literature
    • Nov-Dec; [PubMed]
    • Al Hawsawi K, Al Aboud K, Ramesh V, Al Aboud D. Dyschromatosis universalis hereditaria: report of a case and review of the literature. Pediatr Dermatol. 2002 Nov-Dec;19(6):523-6. [PubMed]
    • (2002) Pediatr Dermatol. , vol.19 , Issue.6 , pp. 523-526
    • Al Hawsawi, K.1    Al Aboud, K.2    Ramesh, V.3    Al Aboud, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.