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Abstract #24638 Published in IGR 11-4
High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucoma
Abu-Amero KK; Hellani A; Bender P; Spaeth GL; Myers J; Katz LJ; Moster M; Bosley TMMolecular Vision 2009; 15: 1594-1598
Purpose: To determine whether patients with isolated primary open-angle glaucoma (POAG) have evidence of chromosomal copy number alterations. Methods: Twenty-seven Caucasian and African-American POAG patients and 12 ethnically matched controls were carefully screened for possible glaucoma and tested for chromosomal copy number alterations using high resolution array comparative genomic hybridization. Results: No POAG patient had evidence of chromosomal copy number alterations when compared to normal ethnically matched controls. Additionally, there was no evidence of somatic mosaicism in any tested POAG patient. Conclusions: Chromosomal deletions and/or duplications were not detected in POAG patients as compared to controls. Other chromosomal imbalances such as translocations, inversions, and some ploidies cannot be detected by current array comparative genomic hybridization technology, and other nuclear genetic, mitochondrial abnormalities, or epigenetic factors cannot be excluded as a possible contributing factor to POAG pathogenesis.
K.K. Abu-Amero. Ophthalmic Genetics Laboratory, Department of Ophthalmology, King Saud University, PO Box 245, Riyadh 11411, Saudi Arabia. abuamero@gmail.com
Classification:
3.5 Molecular biology incl. SiRNA (Part of: 3 Laboratory methods)
