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Trabecular Meshwork-Based MIGS: Efficacy, Technique Variability, and Wound Healing-A Comprehensive Review. [PDF]

J Clin Med
Butt FR, Dhivagaran T, Stasso J, Sachdeva K, Arunasalam L, Abid F, Tao BK, Balas M, Mathew DJ.   +8 more
europepmc   +1 more source

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The inheritance of juvenile onset primary open angle glaucoma

Clinical Genetics, 2017
Juvenile onset open angle glaucoma (JOAG) affects patients before 40 years of age, who present with high intraocular pressure and deep steep cupping of the optic nerve head. While it was considered to be inherited in an autosomal dominant fashion, recent studies have shown an autosomal recessive pattern as well as sporadic occurrence of the disease in ...
, Abadh K Chaurasia
exaly   +3 more sources

Clinical correlates to the goniodysgensis among juvenile-onset primary open-angle glaucoma patients

Graefe's Archive for Clinical and Experimental Ophthalmology, 2013
To evaluate gonioscopic features and relate them to clinical characteristics in eyes with juvenile-onset primary open-angle glaucoma (JOAG).Goniophotographs of unrelated JOAG patients, presenting between 10-40 years of age, were evaluated and compared with 60 healthy subjects in the same age group.
Aparna Rao, John Fingert, Viney Gupta
exaly   +3 more sources

Clinical and Genetic Characteristics of Primary Juvenile-Onset Open-Angle Glaucoma (JOAG)

Seminars in Ophthalmology, 2008
Juvenile-onset open-angle glaucoma (JOAG) is an autosomal dominant disease characterized by an early age of onset and severely elevated intraocular pressures. Large JOAG pedigrees have been pivotal in genetic linkage analyses that have helped establish the association between JOAG and the myocilin gene (MYOC).
TERESA Chen
exaly   +3 more sources

Clinical Phenotype of Juvenile-onset Primary Open-angle Glaucoma Linked to Chromosome 1q

Ophthalmology, 1996
Recent reports have suggested that a gene responsible for juvenile-onset primary open-angle glaucoma exists on the long arm of chromosome 1 (1q). This report describes a previously unpublished family (UM:JG3) in which juvenile-onset glaucoma is segregating in an autosomal dominant manner.
Michael Boehnke, Paul R Lichter, P R Lichter   +2 more
exaly   +3 more sources

Identification of a new ‘TIGR’ mutation in a family with juvenile-onset primary open angle glaucoma

Ophthalmic Genetics, 1997
Positional mapping of families segregating for juvenile-onset primary open angle glaucoma (JOAG) has previously identified a locus (GLCIA) for this condition on the long arm of chromosome I. Recently, three mutations in the TIGR gene (Trabecular meshwork Inducible Gluco-corticoid Response protein) have been described in a total of ten familial, three ...
Mansoor Sarfarazi, B W Fleck, R P Crick
exaly   +3 more sources

Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucoma

Gene, 2015
Glaucoma is one of the primary causes of visual impairment and blindness in the world. It is characterized by the damage to the optic nerve head and visual field loss. Variants in CYP1B1 are the most common cause of glaucoma in different world populations.
Sadaf Naz, Rasheeda Bashir, Shagufta Naz   +2 more
exaly   +3 more sources

Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree,

Ophthalmology, 1998
This study aimed to update a large kindred with juvenile-onset primary open-angle glaucoma (POAG) first described in 1940 and to identify the underlying genetic cause of the disease.Molecular genetic study of a single kindred, including clinical examination, retrospective review of clinical and family history records, linkage analysis, and mutation ...
Debra Thompson, Paul R Lichter, M A Musarella   +2 more
exaly   +3 more sources