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  Vol. 124 No. 9, September 2006 TABLE OF CONTENTS
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  Ophthalmic Molecular Genetics
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The Role of the WDR36 Gene on Chromosome 5q22.1 in a Large Family With Primary Open-Angle Glaucoma Mapped to This Region

Patricia L. Kramer, PhD; John R. Samples, MD; Sharareh Monemi, MD, PhD; Renee Sykes, BS; Mansoor Sarfarazi, PhD; Mary K. Wirtz, PhD

Arch Ophthalmol. 2006;124:1328-1331.

Objective  To determine whether mutations in the WD40-repeat 36 (WDR36) gene are responsible for primary open-angle glaucoma (POAG) that maps to the GLC1G locus in a family with 16 affected family members.

Methods  Ninety-two family members underwent clinical evaluation for POAG on the basis of intraocular pressures, cupping of discs, and visual fields after informed consent was obtained. All 23 exons of WDR36 were sequenced in DNA from 5 affected and 2 unaffected family members.

Results  Sixteen family members showed evidence of POAG. A number of sequence variations were identified in family members; most of the variations were previously described single-nucleotide polymorphisms also present in the general population. The 3 new sequence changes were all intronic; 2 were found in only 1 of the family members undergoing screening.

Conclusions  Several polymorphisms, including known single-nucleotide polymorphisms, were identified; however, none of these were consistent with disease-causing mutations. A mutation in a noncoding region of WDR36 may be responsible for POAG in this family, or another gene in this region may be the actual cause of glaucoma in this family.

Clinical Relevance  The finding that the WDR36 gene is probably not the responsible gene in this family further documents the genetic heterogeneity of POAG.


Author Affiliations: Departments of Neurology (Dr Kramer), Molecular and Medical Genetics (Drs Kramer and Wirtz), and Ophthalmology, Casey Eye Institute (Drs Samples and Wirtz and Ms Sykes), Oregon Health and Sciences University, Portland; and the Molecular Ophthalmic Genetics Laboratory and the Department of Surgery, University of Connecticut Health Center, Farmington (Drs Monemi and Sarfarazi).



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Profiling of WDR36 Missense Variants in German Patients with Glaucoma
Pasutto et al.
IOVS 2008;49:270-274.
ABSTRACT | FULL TEXT  





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