1Keithahn MAZ, Huang M, Keltner JL,et al. The variable expressivity of a family with central areolar pigment epithelial dystrophy. Ophthalmology,1996,103:406-415.
2Small KW, Hernsen V, Gurney N, et,al. North Carolina macular dystrophy and central areolar pigment epithelial dystrophy. Arch Ophthalmol, 1992, 110: 515-518.
3Freeman WR. Practical atlas of retinal disease and therapy. New York: Raven Press, 1993:14-16.
5Francois J, De Rouck A, Cambie E, et al. Visual functions in pericentral and central pigmentary retinopathy[J]. Ophthalmolog- ica, 1972,165 (1) : 38-61.
6Jim6nez-Sierra J M, Ogden T E,Van Boemel G B. Inherited ret- inal diseases:a diagnostic guide[M]. St Louis:Mosby,1989:289.
7Sandberg M A, Gaudio A R, Berson E L. Disease course of pa- tients with pericentral retinitis pigmentosa[J]. American Journal of Ophthalmology, 2005,140( 1 ) : 100-106.
8FERRUCCI S,Anderson S F,Townsend J C. Retinitis pigmento- sa inversa[J]. Optometry Vision Science,1998,75(8):560-570.
9Iijima H, Okajima O, Okamoto M, Tanino T. Central pigmentary retinal dystrophy and its angiographic classification [J]. Jpn J Ophthalmol, 1983,27 (3) : 468-95.
100zdek Z O, Gtirelik G, Bilgihan K, et al. Stargardt's disease and retinitis pigmentosa: different phenotypic presentations in the same family[ J ]. Eye, 2005,19 ( 11 ) : 1222-1225.
