Literature DB >> 23218808

The genetics of pigment dispersion syndrome and pigmentary glaucoma.

Gerassimos Lascaratos1, Ameet Shah, David F Garway-Heath.   

Abstract

We review the inheritance patterns and recent genetic advances in the study of pigment dispersion syndrome (PDS) and pigmentary glaucoma (PG). Both conditions may result from combinations of mutations in more than one gene or from common variants in many genes, each contributing small effects. We discuss the currently known genetic loci that may be related with PDS/PG in humans, the role of animal models in expanding our understanding of the genetic basis of PDS, the genetic factors underlying the risk for conversion from PDS to PG and the relationship between genetic and environmental--as well as anatomical--risk factors.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23218808     DOI: 10.1016/j.survophthal.2012.08.002

Source DB:  PubMed          Journal:  Surv Ophthalmol        ISSN: 0039-6257            Impact factor:   6.048


  12 in total

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Authors:  Teresa Borrás
Journal:  J Ocul Pharmacol Ther       Date:  2014-02-24       Impact factor: 2.671

2.  Radiation pretreatment does not protect the rat optic nerve from elevated intraocular pressure-induced injury.

Authors:  Elaine C Johnson; William O Cepurna; Dongseok Choi; Tiffany E Choe; John C Morrison
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-12-18       Impact factor: 4.799

3.  Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes.

Authors:  Mark J Simcoe; Nicole Weisschuh; Bernd Wissinger; Pirro G Hysi; Christopher J Hammond
Journal:  JAMA Ophthalmol       Date:  2020-03-01       Impact factor: 7.389

Review 4.  Pigment dispersion syndrome and pigmentary glaucoma: overview and racial disparities.

Authors:  Ruiqi Pang; Siloka A Labisi; Ningli Wang
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2022-09-10       Impact factor: 3.535

5.  Iris coloboma in one eye and pigment dispersion syndrome in the fellow eye.

Authors:  Virgilio Galvis; Alejandro Tello; Paul Valarezo; Angélica M Prada
Journal:  BMJ Case Rep       Date:  2013-05-22

6.  Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

Authors:  Chi-Fan Yang; Shuan-Pei Lin; Chien-Ping Chiang; Yu-Hung Wu; Weng Siong H'ng; Chun-Ping Chang; Yuan-Tsong Chen; Jer-Yuarn Wu
Journal:  Am J Hum Genet       Date:  2018-01-11       Impact factor: 11.025

7.  Bilateral acute depigmentation of the iris in two siblings simultaneously.

Authors:  Rana Amin; Amena Nabih; Noha Khater
Journal:  Am J Ophthalmol Case Rep       Date:  2018-03-16

8.  Exome-based investigation of the genetic basis of human pigmentary glaucoma.

Authors:  Carly van der Heide; Wes Goar; Kacie J Meyer; Wallace L M Alward; Erin A Boese; Nathan C Sears; Ben R Roos; Young H Kwon; Adam P DeLuca; Owen M Siggs; Claudia Gonzaga-Jauregui; Val C Sheffield; Kai Wang; Edwin M Stone; Robert F Mullins; Michael G Anderson; Bao Jian Fan; Robert Ritch; Jamie E Craig; Janey L Wiggs; Todd E Scheetz; John H Fingert
Journal:  BMC Genomics       Date:  2021-06-26       Impact factor: 4.547

9.  Pigmentary Glaucoma with Retinochoroidal Pigmentation.

Authors:  Syed Shoeb Ahmad; Shuaibah Abdul Ghani
Journal:  J Ophthalmic Vis Res       Date:  2016 Jan-Mar

10.  What's in a Gene? Pseudoexfoliation Syndrome and Pigment Dispersion Syndrome in the Same Patient.

Authors:  Olya Pokrovskaya; Colm O'Brien
Journal:  Case Rep Ophthalmol       Date:  2016-01-21
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