Pigment-dispersion Syndrome
What's New
Last Posted: Oct 26, 2022
- Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development.
Simcoe Mark J, et al. Ophthalmology 2022 0 (6) 626-636 - Exome-based investigation of the genetic basis of human pigmentary glaucoma.
van der Heide Carly, et al. BMC genomics 2021 6 (1) 477 - Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma.
Giardina Emiliano, et al. BMC ophthalmology 2014 0 (1) 52 - Pigment-dispersion syndrome
From NCATS Genetic and Rare Diseases Information Center - Association of microsatellite polymorphisms of the GPDS1 locus with normal tension glaucoma in the Japanese population.
Nakamura Kayo, et al. Clinical ophthalmology (Auckland, N.Z.) 2009 0 307-12 - Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma.
Rao Kollu Nageswara, et al. Molecular vision 2008 0 1254-62
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