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Volumn 72, Issue 6, 2006, Pages 449-451

Variant of Vohwinkel's syndrome

Author keywords

Keratoderma; Palmoplantar; Vohwinkel's syndrome

Indexed keywords

LORICRIN;

EID: 33845949593     PISSN: 03786323     EISSN: None     Source Type: Journal    
DOI: 10.4103/0378-6323.29344     Document Type: Article
Times cited : (9)

References (11)
  • 1
    • 0001245331 scopus 로고
    • Keratoderma hereditarium meditans
    • Vohwinkel KH. Keratoderma hereditarium meditans. Arch Dermatol Syphil 1929;158:354-64.
    • (1929) Arch Dermatol Syphil , vol.158 , pp. 354-364
    • Vohwinkel, K.H.1
  • 2
    • 0021174720 scopus 로고
    • Variant of Keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin
    • Camisa C, Rossana C. Variant of Keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin. Arch Dermatol 1984;120:1323-8.
    • (1984) Arch Dermatol , vol.120 , pp. 1323-1328
    • Camisa, C.1    Rossana, C.2
  • 3
    • 0019428104 scopus 로고    scopus 로고
    • Chang Sing Pang AF, Oranje AP, Vuzevki VD, Stolz E. Successful treatment of keratoderma hereditaria mutilans with an aromatic retinoid. Arch Dermatol 1981;117:225-8.
    • Chang Sing Pang AF, Oranje AP, Vuzevki VD, Stolz E. Successful treatment of keratoderma hereditaria mutilans with an aromatic retinoid. Arch Dermatol 1981;117:225-8.
  • 4
    • 0013965847 scopus 로고
    • Keratoderma hereditaria mutilans (Vohwinkel): Differentiating features of conditions with constriction of digits
    • Gibbs RC, Frank SB. Keratoderma hereditaria mutilans (Vohwinkel): Differentiating features of conditions with constriction of digits. Arch Dermatol 1966;94:619-25.
    • (1966) Arch Dermatol , vol.94 , pp. 619-625
    • Gibbs, R.C.1    Frank, S.B.2
  • 6
    • 0032790899 scopus 로고    scopus 로고
    • A missense mutation in connexim 26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
    • Maestrini E, Korge BP, Ocana-Sierra J, Calzolari E, Cambiaghi S, Scudder PM, et al. A missense mutation in connexim 26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. Hum Mol Genet 1999;8:1237-43.
    • (1999) Hum Mol Genet , vol.8 , pp. 1237-1243
    • Maestrini, E.1    Korge, B.P.2    Ocana-Sierra, J.3    Calzolari, E.4    Cambiaghi, S.5    Scudder, P.M.6
  • 8
    • 15844391073 scopus 로고    scopus 로고
    • A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
    • Maestrini E, Monaco AP, McGrath JA, Ishida-Yamamoto A, Camisa C, Hovnanian A, et al. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nat Genet 1996;13:70-7.
    • (1996) Nat Genet , vol.13 , pp. 70-77
    • Maestrini, E.1    Monaco, A.P.2    McGrath, J.A.3    Ishida-Yamamoto, A.4    Camisa, C.5    Hovnanian, A.6
  • 9
    • 0028933496 scopus 로고
    • Keratoderma hereditaria mutilans (Vohwinkel's syndrome) associated with congenital deaf mutism
    • Peris K, Salvati EF, Torlone G, Chimenti S. Keratoderma hereditaria mutilans (Vohwinkel's syndrome) associated with congenital deaf mutism. Br J Dermatol 1995;132:617-20.
    • (1995) Br J Dermatol , vol.132 , pp. 617-620
    • Peris, K.1    Salvati, E.F.2    Torlone, G.3    Chimenti, S.4
  • 10
    • 0021687216 scopus 로고
    • Mutilating palmoplantar keratoderma successfully treated with etretinate
    • Wereide K. Mutilating palmoplantar keratoderma successfully treated with etretinate. Acta Derm Venerol 1984;64:566-9.
    • (1984) Acta Derm Venerol , vol.64 , pp. 566-569
    • Wereide, K.1
  • 11
    • 0021833186 scopus 로고
    • Etretinate: Management of keratoma hereditaria mutilans in four family members
    • Rivers JK, Duke EE, Justus DW. Etretinate: Management of keratoma hereditaria mutilans in four family members. J Am Acad Dermatol 1985;13:43-9.
    • (1985) J Am Acad Dermatol , vol.13 , pp. 43-49
    • Rivers, J.K.1    Duke, E.E.2    Justus, D.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.