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Volumn 156, Issue 1, 2007, Pages 196-198

Spotted and rippled reticulate hypermelanosis: A possible variant of Dowling-Degos disease [19]

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DOWLING DEGOS DISEASE; ELECTRON MICROSCOPY; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERMELANOSIS; HYPERPIGMENTATION; IMAGE ANALYSIS; JAPANESE; LETTER; MELANOSIS; ONSET AGE; PIGMENT DISORDER; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN BIOPSY; STAINING; SYMPTOM;

EID: 33845515481     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2006.07592.x     Document Type: Letter
Times cited : (9)

References (8)
  • 1
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    • Disorders of skin colour
    • (Burns T, Breathnach SM, Cox NH, Griffiths CEM, eds), 7th edn, Oxford: Blackwell Publishing
    • Bleehen SS, Anstey AV. Disorders of skin colour. In: Rook's Textbook of Dermatology (Burns T, Breathnach SM, Cox NH, Griffiths CEM, eds), 7th edn, Vol. 2. Oxford: Blackwell Publishing, 2004; 39.13-39.15.
    • (2004) Rook's Textbook of Dermatology , vol.2
    • Bleehen, S.S.1    Anstey, A.V.2
  • 2
    • 33344472840 scopus 로고    scopus 로고
    • Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease
    • Betz RC, Planko L, Eigelshoven S et al. Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease. Am J Hum Genet 2006; 78:510-5.
    • (2006) Am J Hum Genet , vol.78 , pp. 510-515
    • Betz, R.C.1    Planko, L.2    Eigelshoven, S.3
  • 3
    • 7244242474 scopus 로고    scopus 로고
    • Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family
    • Sandhu K, Saraswat A, Kanwar AJ. Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family. J Eur Acad Dermatol Venereol 2004; 18:702-4.
    • (2004) J Eur Acad Dermatol Venereol , vol.18 , pp. 702-704
    • Sandhu, K.1    Saraswat, A.2    Kanwar, A.J.3
  • 5
    • 0027425268 scopus 로고
    • Reticulate acropigmentation of Kitamura: Two case reports
    • Erel A, Gurer ML, Edali N. Reticulate acropigmentation of Kitamura: two case reports. Int J Dermatol 1993; 32:726-7.
    • (1993) Int J Dermatol , vol.32 , pp. 726-727
    • Erel, A.1    Gurer, M.L.2    Edali, N.3
  • 6
    • 0036672388 scopus 로고    scopus 로고
    • Reticulate acropigmentation of Kitamura-Dowling Degos disease overlap: A case report
    • Al-Hawsawi K, Al-Aboud K, Alfadley A, Al-Aboud D. Reticulate acropigmentation of Kitamura-Dowling Degos disease overlap: a case report. Int J Dermatol 2002; 41:518-20.
    • (2002) Int J Dermatol , vol.41 , pp. 518-520
    • Al-Hawsawi, K.1    Al-Aboud, K.2    Alfadley, A.3    Al-Aboud, D.4
  • 7
    • 0031978684 scopus 로고    scopus 로고
    • Overlap of reticulate acropigmentation of Kitamura, acropigmentation of Dohi and Dowling-Degos disease in four generations
    • Thami GP, Jaswal R, Kanwar AJ et al. Overlap of reticulate acropigmentation of Kitamura, acropigmentation of Dohi and Dowling-Degos disease in four generations. Dermatology 1998; 196:350-1.
    • (1998) Dermatology , vol.196 , pp. 350-351
    • Thami, G.P.1    Jaswal, R.2    Kanwar, A.J.3
  • 8
    • 33745565753 scopus 로고    scopus 로고
    • A gene locus responsible for reticulate pigmented anomaly of the flexures maps to chromosome 17p13.3
    • Li CR, Xing QH, Li M et al. A gene locus responsible for reticulate pigmented anomaly of the flexures maps to chromosome 17p13.3. J Invest Dermatol 2006; 126:1297-301.
    • (2006) J Invest Dermatol , vol.126 , pp. 1297-1301
    • Li, C.R.1    Xing, Q.H.2    Li, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.