Literature DB >> 8088822

Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees.

J L Wiggs1, J L Haines, C Paglinauan, A Fine, C Sporn, D Lou.   

Abstract

Glaucoma is a common disorder that results in irreversible damage to the optic nerve, causing absolute blindness. In most cases, the optic nerve is damaged by an elevation of the intraocular pressure that is the result of an abnormality in the normal drainage function of the trabecular meshwork. A family history of glaucoma is an important risk factor for the disease, suggesting that genetic defects predisposing to this condition are likely. Three pedigrees segregating an autosomal dominant juvenile glaucoma demonstrated significant linkage to a group of closely spaced markers on chromosome 1. These results confirm the initial mapping of this disease and suggest that this region on chromosome 1 contains an important locus for juvenile glaucoma. We describe recombination events that improve the localization of the responsible gene, reducing the size of the candidate region from 30 to 12 cM.

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Year:  1994        PMID: 8088822     DOI: 10.1006/geno.1994.1269

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  28 in total

1.  Clinical and genetic characterization of a large primary open angle glaucoma pedigree.

Authors:  Mohideen Abdul Kader; Prasanthi Namburi; Sarika Ramugade; R Ramakrishnan; Subbiah R Krishnadas; Ben R Roos; Sundaresan Periasamy; Alan L Robin; John H Fingert
Journal:  Ophthalmic Genet       Date:  2016-06-29       Impact factor: 1.803

Review 2.  Glaucoma-associated myocilin: a better understanding but much more to learn.

Authors:  Zachary T Resch; Michael P Fautsch
Journal:  Exp Eye Res       Date:  2008-08-29       Impact factor: 3.467

3.  Confirmation of linkage to 1q21-31 in a Danish autosomal dominant juvenile-onset glaucoma family and evidence of genetic heterogeneity.

Authors:  C Graff; S F Urbak; T Jerndal; C Wadelius
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

4.  A second locus for Rieger syndrome maps to chromosome 13q14.

Authors:  J C Phillips; E A del Bono; J L Haines; A M Pralea; J S Cohen; L J Greff; J L Wiggs
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

5.  Genetic heterogeneity of primary open angle glaucoma and ocular hypertension: linkage to GLC1A associated with an increased risk of severe glaucomatous optic neuropathy.

Authors:  A P Brézin; A Béchetoille; P Hamard; F Valtot; M Berkani; A Belmouden; M F Adam; S Dupont de Dinechin; J F Bach; H J Garchon
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

Review 6.  The genetics of primary open angle glaucoma.

Authors:  A Booth; A Churchill; R Anwar; M Menage; A Markham
Journal:  Br J Ophthalmol       Date:  1997-05       Impact factor: 4.638

Review 7.  The genetics of complex ophthalmic disorders.

Authors:  K Evans; A C Bird
Journal:  Br J Ophthalmol       Date:  1996-08       Impact factor: 4.638

Review 8.  Molecular genetics of the glaucomas: mapping of the first five "GLC" loci.

Authors:  V Raymond
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

9.  Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q.

Authors:  M K Wirtz; J R Samples; P L Kramer; K Rust; J R Topinka; J Yount; R D Koler; T S Acott
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

Review 10.  Prospects for genetic intervention in primary open-angle glaucoma.

Authors:  M K Wirtz; T S Acott; J R Samples; J C Morrison
Journal:  Drugs Aging       Date:  1998-11       Impact factor: 3.923

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