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Axenfeld-Rieger syndrome

Known as: Rieger syndrome 
 
National Institutes of Health

Papers overview

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2017
2017
Axenfeld-Rieger syndrome is a rare autosomal dominant condition. Anomalies include anterior segment dysgenesis of the eye, dental… Expand
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Review
2017
Review
2017
ABSTRACT Anterior segment dysgeneses are developmental anomalies of the anterior eye segment that can occur as isolated defects… Expand
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2016
2016
Pitx2 is a conserved homeodomain transcription factor that has multiple functions during embryonic development. Mutations in… Expand
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2016
2016
Axenfeld-Rieger syndrome is a congenital disease with an estimated prevalence of one in 200,000 individuals. This is an… Expand
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Review
2015
Review
2015
Purpose To describe clinical findings in a Korean family with Axenfeld-Rieger syndrome. Methods A retrospective review of… Expand
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2014
2014
Axenfeld-Rieger syndrome (ARS) is an autosomal dominant disorder with variable expressivity. It is characterized by dysgenesis of… Expand
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2014
2014
The purpose of this case report is to report the orthodontic surgical treatment and subsequent dental rehabilitation in two… Expand
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2013
2013
Axenfeld-Rieger syndrome (ARS) is characterized by anomalies of the anterior segment of the eye and systemic abnormalities… Expand
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2012
2012
PURPOSE The homeobox transcription factor PITX2 is a known regulator of mammalian ocular development, and human PITX2 mutations… Expand
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2009
2009
Axenfeld-Rieger syndrome (ARS) is associated with ocular and systemic anomalies. PITX2 is known to be a major controlling gene in… Expand
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