Autosomal dominant Stargardt-like macular dystrophy (ADSLD) is an early-onset form of macular degeneration. ADSLD is one of several heterogeneous causes of macular atrophy in association with subretinal deposits that leads to blindness. ADSLD is of particular interest because of the mutated gene's important role in macular function and phenotypic overlap with age-related macular degeneration (AMD). The long-term goals of this research are to better understand the etiologies and pathophysiologies of macular degenerations. Macular degenerations and dystrophies are common causes of blindness worldwide and the leading cause in older Americans. Heredity plays a major role, not only in the early-onset forms, but also in the more common later-onset macular degenerations. There is no effective treatment for the vast majority of patients. The study of early-onset hereditary macular diseases, such as ADSLD, will provide new knowledge of retinal function and an improved understanding of the pathophysiology of hereditary macular degeneration. The immediate goals of this application are to test the hypothesis that patients with ADSLD linked to chromosome 6 are related through a common founder by genetic and genealogical investigation; to identify and characterize the ADSLD gene; to begin to understand its sites of expression and function; and to determine if the ADSLD gene is involved in a proportion of late AMD.
| Tantri, Avinash; Vrabec, Tamara R; Cu-Unjieng, Andrew et al. (2004) X-linked retinoschisis: a clinical and molecular genetic review. Surv Ophthalmol 49:214-30 |
| Jiao, Xiaodong; Ritter 3rd, Robert; Hejtmancik, J Fielding et al. (2004) Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36. Invest Ophthalmol Vis Sci 45:4498-503 |
| Donoso, Larry A; Hageman, Gregory; Frost, Arcilee et al. (2003) Autosomal dominant macular dystrophy in a large Canadian family. Can J Ophthalmol 38:33-40 |
| Vrabec, Tamara R; Tantri, Avinash; Edwards, Albert et al. (2003) Autosomal dominant Stargardt-like macular dystrophy: identification of a new family with a mutation in the ELOVL4 gene. Am J Ophthalmol 136:542-5 |
| Lee, Mike M; Ritter 3rd, Robert; Hirose, Tatsuo et al. (2003) Snowflake vitreoretinal degeneration: follow-up of the original family. Ophthalmology 110:2418-26 |
| Donoso, Larry A; Edwards, Albert O; Frost, Arcilee T et al. (2003) Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 gene. Surv Ophthalmol 48:191-203 |
| Tantri, Avinash; Vrabec, Tamara R; Cu-Unjieng, Andrew et al. (2003) X-linked retinoschisis: report of a family with a rare deletion in the XLRS1 gene. Am J Ophthalmol 136:547-9 |
| Donoso, Larry A; Edwards, Albert O; Frost, Arcilee T et al. (2002) Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome family. Am J Ophthalmol 134:720-7 |
| Pager, C K; Sarin, L K; Federman, J L et al. (2001) Malattia leventinese presenting with subretinal neovascular membrane and hemorrhage. Am J Ophthalmol 131:517-8 |
| Chung, G W; Edwards, A O; Schimmenti, L A et al. (2001) Renal-coloboma syndrome: report of a novel PAX2 gene mutation. Am J Ophthalmol 132:910-4 |
Showing the most recent 10 out of 15 publications
