Keyword

microcornea

Description: Microcornea is a congenital ocular condition in which the cornea is abnormally small, often occurring with other eye abnormalities.

Primary topic: Ocular Disorders and Treatments (51%)

Wikidata ID: wiki/Q11835146

OpenAlex ID: keywords/microcornea

White-to-White Corneal Diameter

2005 · Florian R??fer, Anke Schr??der, et al. · Cornea · 353

Domain disruption and mutation of the bZIP transcription factor, MAF,associated with cataract, ocular anterior segment dysgenesis and coloboma

2002 · R. V. Jamieson · Human Molecular Genetics · 269

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A review of the ocular manifestations

1997 · D. J. Colville, Judy Savige · Ophthalmic Genetics · 229

Ocular abnormalities in Alagille syndrome11None of the authors has any commercial interest arising from the findings presented in this article.

1999 · Melanie Hingorani, Ken K Nischal, et al. · Ophthalmology · 175

Simple Microphthalmos

1989 · Avery H. Weiss · Archives of Ophthalmology · 172

Frequency and predictors of glaucoma after pediatric cataract surgery

2003 · Peter K. Rabiah · American Journal of Ophthalmology · 167

Glaucoma Following Childhood Cataract Surgery/Discussion

1994 · Monte D Mills, Richard M Robb, et al. · Journal of Pediatric Ophthalmology & Strabismus · 148

Genetic Heterogeneity in Microcornea-Cataract: Five Novel Mutations in CRYAA , CRYGD , and GJA8

2007 · Lars Hansen, Wenliang Yao, et al. · Investigative Ophthalmology & Visual Science · 134

5-year outcomes after primary intraocular lens implantation in children aged 2 years or younger with congenital or infantile cataract: findings from the IoLunder2 prospective inception cohort study

2018 · Ameenat Lola Solebo, Phillippa Cumberland, et al. · The Lancet Child & Adolescent Health · 133

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Phacoemulsification in eyeswith posterior polar cataract

1999 · Abhay Vasavada, Raminder Singh · Journal of Cataract & Refractive Surgery · 112

Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene

2000 · Lisiane B. Meira, John M. Graham, et al. · The American Journal of Human Genetics · 111

Autosomal Recesssive Microcephaly, Microcornea, Congenital Cataract, Mental Retardation, Optic Atrophy, and Hypogenitalism

1993 · Mette Warburg · American journal of diseases of children · 111

Comprehensive Mutational Screening in a Cohort of Danish Families with Hereditary Congenital Cataract

2009 · Lars Hansen, Annemette Mikkelsen, et al. · Investigative Ophthalmology & Visual Science · 106

A Molecular Analysis of the Yemenite Deaf-Blind Hypopigmentation Syndrome: SOX10 Dysfunction Causes Different Neurocristopathies

1999 · N. Bondurand, K. Kuhlbrodt, et al. · Human Molecular Genetics · 106

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Oculodentodigital Dysplasia

1979 · G. Frank Judisch · Archives of Ophthalmology · 104

Secondary glaucoma after paediatric cataract surgery

2007 · B N Swamy, F Billson, et al. · British Journal of Ophthalmology · 101

Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly

2004 · R Richardson, D Donnai, et al. · Journal of Medical Genetics · 101

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Corneal Abnormalities in Ehlers-Danlos Syndrome Type VI

1993 · James A. Cameron · Cornea · 98

Marfan's Syndrome

1942 · ANDREW RADOS · Archives of ophthalmology · 94

Visual impairment and ocular abnormalities in children with fetal alcohol syndrome

2004 · Kerstin Strömland · Addiction Biology · 92

Ocular and Orbital Manifestations of the Inherited Bone Marrow Failure Syndromes: Fanconi Anemia and Dyskeratosis Congenita

2009 · Ekaterini T. Tsilou, Neelam Giri, et al. · Ophthalmology · 91

Visual acuity in children with coloboma

2000 · Stella J Hornby, Shajan Adolph, et al. · Ophthalmology · 91

Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.

2002 · Ordan J Lehmann, Neil D Ebenezer, et al. · PubMed · 90

Corneal Diameter in Childhood Aphakic Glaucoma

1996 · David K Wallace, David A Plager · Journal of Pediatric Ophthalmology & Strabismus · 90

A novel mutation in the DNA‐binding domain of MAF at 16q23.1 associated with autosomal dominant “cerulean cataract” in an Indian family

2006 · Vanita Vanita, Daljit Singh, et al. · American Journal of Medical Genetics Part A · 89

Works count: 759

Citation count: 10,140