国际皮肤性病学杂志    2005 31 (4): 223-225   ISSN: 2096-5540  CN: 32-1880/R   点状掌跖角化病研究进展 李明1, 杨莉佳1, 张学军2 1. 南京医科大学附属无锡第二医院、无锡市第二人民医院皮肤科, 无锡214002; 2. 安徽医科大学第一附属医院皮肤科、安徽医科大学皮肤病研究所 收稿日期 2004-08-24  修回日期 null  网络版发布日期 null 参考文献  [1] Gupta R, Mehta S, Pandhi D,et al. Hereditary Punctate Palmoplantar Keratoderma (PPK) (Brauer-Buschke-Fischer Syndrome). J Dermatolm, 2004, 31:398-402. [2] Emmert S, Kuster W, Hennies HC, et al. 47 patients in 14 families with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer. Eur J Dermatol, 2003, 13:16-20. [3] Stanimirovic A, Kansky A, Basta-Juzbasic A, et al. Hereditary palmoplantar keratoderma, type papulosa, in Croatia. J Am Acad Dermatol, 1993, 29:435-437. [4] Zhang X J, Li M, Gao TW, et al. Identification of a locus for punctate palmoplantar keratodermas at chromosome 8q24.13-8q24.21. J Invest Dermatol, 2004, 122:1121-1125. [5] Wong SS, Tan KG, Goh CL. Cutaneous manifestations of chronic arsenicism: review of seventeen cases. J Am Acad Dermatol, 1998,38:179-185. [6] Col M, Col C, Soran A, et al. Arsenic-related Bowen's disease, palmar keratosis, and skin cancer. Environ Health Perspect, 1999,107:687-689. [7] Watson K, Creamer D. Arsenic-induced keratoses and Bowen's disease. Clin Exp Dermatol, 2004, 29:46-48. [8] Wei SC, Yang S, Li M, et al. Identification of a locus for porokeratosis palmaris et plantaris disseminata to a 6.9-cM region at chromosome 12q24.1-24.2. Br J Dermatol, 2003, 149:261-267. [9] Bogle MA, Hwang LY, Tschen JA. Acrokeratoelastoidosis. J Am Acad Dermatol, 2002, 47:448-451. [10] Stevens HP, Kelsell DP, Leigh IM, et al. Punctate palmoplantar keratoderma and malignancy in a four-generation family. Br J Dermatol,1996, 134:720-726. [11] Kelsell DP, Stevens HP, Ratnavel R, et al. Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity. Hum Mol Genet, 1995, 4:1021-1025. [12] Martinez-Mir A, Zlotogorski A, Londono D, et al. Identification of a locus for type Ⅰ punctate palmoplantar keratoderma on chromosome15q22-q24. J Med Genet, 2003, 40:872-878. [13] Lee YG, Macoska JA, Korenchuk S,et al. MIM, a potential metastasis suppressor gene in bladder cancer. Neoplasia, 2002, 4: 291-294. [14] Hesse S, Berbis P, Privat Y. Keratodermia palmo-plantaris papulosa(Buschke-Fischer's disease): efficacy of acitretin. Br J Dermatol,1993, 128:104-105. [15] Powell FC, Venencie PY, Gordon H, et al. Keratoderma and spastic paralysis. Br J Dermatol, 1983, 109:589-596. [16] Gamborg Nielsen P. Punctate palmoplantar keratoderma associated with morbus Bechterew and HLA B 27. A family study. Acta Derm Venereol, 1988, 68:346-350. [17] Salamon T, Stolic V, Lazovic-Tepavac O, et al. Peculiar findings in a family with keratodermia palmo-plantaris papulosa Buschke-FischerBrauer. Hum Genet, 1982, 60:314-319. [18] Emmert S, Kuster W, Zutt M, et al. A new family with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.J Am Acad Dermatol, 2003, 49:1166-1169. [19] Asadi AK. Type Ⅰ hereditary punctate keratoderma. Dermatol OnlineJ, 2003, 9:38. [20] Kelsell DP, Stevens HP. The palmoplantar keratodermas: much more than palms and soles. Mol Med Today,1999, 5:107-113. 通讯作者: