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[1] Patrizi A, Manneschi V, Pini A, et al. Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report.Acta Derm Venereol, 1994, 74:135-137. [2] Alfadley A, Al Ajlan A, Hainau B, et al. Reticulate acropigmentation of Dohi: a case report of autosomal recessive inheritance. J Am Acad Dermatol, 2000, 43: 113-117. [3] Urabe K, Hori Y. Dyschromatosis. Semin Cutan Med Surg, 1997,16:81-85. [4] Zhang X J, Gao M, Li M, et al. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21. J Invest Dermatol, 2003, 120: 776-780. [5] Xing QH, Wang MT, Chen XD, et al. A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome [6] q24.2-q25.2. Am J Hum Genet, 2003, 73:377-382.6.Dhar S, Malakar S. Acropigmentation of Dohi in a 12-year-old boy.Pediatr Dermatol, 1998, 15: 242. [7] Henanthkumar, Thappa DM. Dyschromatosis symmetrica hereditaria in an Indian family. J Dermatol, 1999, 26:544-545. [8] Tan HH, Tay YK. Neurofibromatosis and reticulate acropigmentation of Dohi: a case report. Pediatr Dermatol, 1997, 14:296-298. [9] Tojyo K, Hattori T, Sekijima Y,et al. A case of idiopathic brain calcification associated with dyschromatosis symmetrica hereditaria, aplasia of dental root, and aortic valve sclerosis. Rinsho Shinkeigaku,2001, 41: 299-305. [10] Oyama M, Shimizu H, Ohata Y, et al. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases. Br J Dermatol, 1999, 140:491-496. [11] Danese P, Zanca A, Bertazzoni MG. Familial reticulate acropigmentation of Dohi. J Am Acad Dermatol, 1997, 37:884-886. [12] Hata S, Yokomi I. Density of dopa-positive melanocytes in dyschromatosis symmetrica hereditaria. Dermatologica, 1985, 171: 27-29. [13] Al Hawsawi K, Al Aboud K, Ramesh V, et al. Dyschromatosis universalis hereditaria: report of a case and review of the literature. Pediatr Dermatol, 2002, 19: 523-526. [14] Dhar S, Malakar S. Localized form of dyschromatosis universalis hereditaria in a 14-year-old girl. Pediatr Dermatol, 1999, 16 (4):336. [15] A1 Hawsawi K, A1 Aboud K, Alfadley A, et al. Reticulate acropigmentation of Kitamura-Dowling Degos disease overlap: a case report.Int J Dermatol, 2002, 41: 518-520. [16] 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, 196:350-351. [17] Ohtoshi E, Matsunura Y, Nishigori C,et al. Useful applications of DNA repair tests for differential diagnosis of atypical dyschromatosis symmetrica hereditaria from xeroderma pigmentosum. Br J Dermatol,2001, 144: 162-168. [18] Rapic-Otrin V, Navazza V, Nardo T, et al. True XP group E patients have a defective UV-damaged DNA binding protein complex and mutations in DDB2 which reveal the functional domains of its p48 product.Hum Mol Genet, 2003, 12:1507-1522. [19] Schnur RE, Heymann WR. Reticulate hyperpigmentation. Semin Cutan Med Surg, 1997, 16:72-80. [20] Taki T, Kozuka S, Izawa Y, et al. Surgical treatment of speckled skin caused by dyschromatosis symmetrica hereditaria-case report. J Dermatol, 1986, 13:471-473. [21] Kono M, Miyamura Y, Matsunaga J, et al. Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9. J Dermatol Sci, 2000, 22:88-95. |
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