Natural History of Phenotypic Changes in Stargardt Macular Dystrophy

被引:78
|
作者
Walia, Saloni [1 ]
Fishman, Gerald A. [1 ]
机构
[1] Univ Illinois, Dept Ophthalmol & Visual Sci, Chicago, IL 60612 USA
关键词
Stages of Stargardt macular dystrophy; visual acuity in Stargardt disease; VISUAL-ACUITY LOSS; FUNDUS-FLAVIMACULATUS; FOLLOW-UP; DISEASE; GENE; MAPS;
D O I
10.1080/13816810802695550
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Stargardt macular dystrophy is the most common form of juvenile onset macular degeneration. This article reviews the four stages through which this dystrophy may progress. Also, reviewed here are the variations that may be observed in the visual acuity of patients with Stargardt disease.
引用
收藏
页码:63 / 68
页数:6
相关论文
共 50 条
  • [41] Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy
    Hubbard, AF
    Askew, EW
    Thompson, CJ
    Singh, N
    Leppert, M
    Berstein, PS
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 : U715 - U715
  • [42] Preferred retinal locus and directional reference in patients with Stargardt's macular dystrophy.
    Reinhard, J
    Scholl, HP
    Trauzettel-Klosinski, S
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (04) : S814 - S814
  • [43] Clinical characteristics of autosomal dominant Stargardt's macular dystrophy with genetic linkage to chromosome
    Zhang, K
    Ferraro, A
    Kniazeva, M
    Han, M
    Donoso, LA
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1997, 38 (04) : 4448 - 4448
  • [44] Progression of Atrophy of the Retinal Pigment Epithelium in Stargardt Macular Dystrophy on Fundus Autofluorescence Imaging
    Fletcher, Emily
    Wolfson, Yulia
    Munoz, Beatriz
    Scholl, Hendrik
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2013, 54 (15)
  • [45] Analysis of the nucleotide binding domains of ABCR. the protein defective in stargardt macular dystrophy
    Ahn, J
    Bungert, S
    Molday, LL
    Molday, RS
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2002, 43 : U313 - U313
  • [46] Autosomal dominant Stargardt-like macular dystrophy segregating in a large Canadian family
    Lagali, PS
    MacDonald, IM
    Griesinger, IB
    Chambers, ML
    Ayyagari, R
    Wong, PW
    CANADIAN JOURNAL OF OPHTHALMOLOGY-JOURNAL CANADIEN D OPHTALMOLOGIE, 2000, 35 (06): : 315 - 324
  • [47] Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophy
    Indelman, M
    Hamel, CP
    Bergman, R
    Nischal, KK
    Thompson, D
    Surget, MO
    Ramon, M
    Ganthos, H
    Miller, B
    Richard, G
    Lurie, R
    Leibu, R
    Russell-Eggitt, I
    Sprecher, E
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (05) : 1217 - 1220
  • [48] Phenotypic description of a new feline retinopathy for macular dystrophy studies
    Petersen-Jones, Simon M.
    Occelli, Laurence Mireille
    Minella, Andrea L.
    Querubin, Janice R.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)
  • [49] Investigation of the effect of dietary docosahexaenoic acid (DHA) supplementation on macular function in subjects with autosomal recessive Stargardt macular dystrophy
    MacDonald, Ian M.
    Sieving, Paul A.
    OPHTHALMIC GENETICS, 2018, 39 (04) : 477 - 486
  • [50] Yearly Loss of Retinal Thickness and Macular Volume Estimated from SPECTRALIS OCT Measurements in Patients with Stargardt Macular Dystrophy
    Strauss, Rupert
    Fletcher, Emily
    Wolfson, Yulia
    Scholl, Hendrik
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2013, 54 (15)