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Journal of the American Academy of Dermatology
Volumn 61, Issue 4, 2009, Pages 725-727
Hyperpigmented, hypertrichotic, and sclerodermoid plaques: An unusual variant of Muckle-Wells syndrome
Author keywords

[No Author keywords available]
Indexed keywords

AMYLOID PROTEIN; C REACTIVE PROTEIN; COLCHICINE; INTERLEUKIN 6;
EID: 70149106348     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaad.2009.03.020     Document Type: Letter
Times cited : (5)
References (7)
  • 1
    • 45049088360 scopus 로고    scopus 로고
    • The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations
    • Molho-Pessach V., Agha Z., Aamar S., Glaser B., Doviner V., Hiller N., et al. The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations. J Am Acad Dermatol 59 (2008) 79-85
    • (2008) J Am Acad Dermatol , vol.59 , pp. 79-85
    • Molho-Pessach, V.1    Agha, Z.2    Aamar, S.3    Glaser, B.4    Doviner, V.5    Hiller, N.6
  • 2
    • 33646067415 scopus 로고    scopus 로고
    • Autosomal recessive plasma cell paniculitis with morphea-like clinical manifestation
    • Hamadah I.R., and Banka N. Autosomal recessive plasma cell paniculitis with morphea-like clinical manifestation. J Am Acad Dermatol 54 suppl (2006) S189-S191
    • (2006) J Am Acad Dermatol , vol.54 , Issue.SUPPL
    • Hamadah, I.R.1    Banka, N.2
  • 4
    • 33947686755 scopus 로고    scopus 로고
    • Pigmented hypertrichotic dermatosis and insulin dependent diabetes: manifestations of a unique genetic disorder?
    • Prendiville J., Rogers M., Kan A., de Castro F., Wong M., Junker A., et al. Pigmented hypertrichotic dermatosis and insulin dependent diabetes: manifestations of a unique genetic disorder?. Pediatr Dermatol 24 (2006) 101-107
    • (2006) Pediatr Dermatol , vol.24 , pp. 101-107
    • Prendiville, J.1    Rogers, M.2    Kan, A.3    de Castro, F.4    Wong, M.5    Junker, A.6
  • 5
    • 33644768091 scopus 로고    scopus 로고
    • Muckle-Wells syndrome: report of six cases with hyperpigmented sclerodermoid skin lesions
    • El-Darouti M.A., Marzouk S.A., and Abdel-Halim M.R. Muckle-Wells syndrome: report of six cases with hyperpigmented sclerodermoid skin lesions. Int J Dermatol 45 (2006) 239-244
    • (2006) Int J Dermatol , vol.45 , pp. 239-244
    • El-Darouti, M.A.1    Marzouk, S.A.2    Abdel-Halim, M.R.3
  • 6
    • 0026777433 scopus 로고
    • Increased osteoclast development after estrogen loss: mediation by interleukin-6
    • Jilka R.L., Hangoc G., Girasole G., Passeri G., Williams D.C., Abrams J.S., et al. Increased osteoclast development after estrogen loss: mediation by interleukin-6. Science 257 (1992) 88-91
    • (1992) Science , vol.257 , pp. 88-91
    • Jilka, R.L.1    Hangoc, G.2    Girasole, G.3    Passeri, G.4    Williams, D.C.5    Abrams, J.S.6
  • 7
    • 0028149351 scopus 로고
    • Autosomal dominant Muckle-Wells syndrome associated with cystinuria, ichthyosis, and aphthosis in a four-generation family
    • Berthelot J.M., Maugars Y., Robillard N., Pascal O., Stalder J.F., David A., et al. Autosomal dominant Muckle-Wells syndrome associated with cystinuria, ichthyosis, and aphthosis in a four-generation family. Am J Med Genet 53 (1994) 72-74
    • (1994) Am J Med Genet , vol.53 , pp. 72-74
    • Berthelot, J.M.1    Maugars, Y.2    Robillard, N.3    Pascal, O.4    Stalder, J.F.5    David, A.6

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.