Irido-corneo-trabecular dysgenesis (disorder)

Known as: Peter anomaly, Peter's anomaly, peters' anomaly 
A form of anterior segment dysgenesis in which abnormal cleavage of the anterior chamber occurs. Peters anomaly is characterized by central… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1952-2017
051019522016

Papers overview

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2006
2006
PURPOSE Peters anomaly is a developmental anomaly of the eye frequently associated with glaucoma. The aim of this study was to… (More)
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Walker-Warburg syndrome (WWS) is an autosomal recessive condition characterised by congenital muscular dystrophy… (More)
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2005
2005
The human PITX3 gene encodes a bicoid-like homeodomain transcription factor associated with a variety of congenital ocular… (More)
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2005
2005
Background: Walker-Warburg syndrome (WWS) is an autosomal recessive condition characterised by congenital muscular dystrophy… (More)
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Highly Cited
2003
Highly Cited
2003
The PAX6 gene is involved in ocular morphogenesis and is expressed in the developing central nervous system and numerous ocular… (More)
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2003
2003
PURPOSE Mutations of the forkhead transcription factor gene FOXC1 result in anterior segment anomalies. No description of the… (More)
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2002
2002
PURPOSE To determine the distribution of CYP1B1 gene mutations in Brazilian patients with primary congenital glaucoma (PCG… (More)
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1999
1999
The PAX6 gene is involved in ocular morphogenesis, and PAX6 mutations have been detected in various types of ocular anomalies… (More)
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1998
1998
PAX6 is a transcription factor with two DNA-binding domains (paired box and homeobox) and a proline-serine-threonine (PST)-rich… (More)
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1995
1995
Autosomal dominant keratitis (ADK) is an eye disorder chiefly characterized by corneal opacification and vascularization and by… (More)
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