Rieger syndrome

Known as: axenfeld syndrome, Iridogoniodysgenesis with somatic anomalies, riegers syndrome 
A congenital malformation of the anterior segment characterized by iridicorneal malformation, glaucoma, iris stroma hypoplasia, posterior embryotoxon… (More)
National Institutes of Health

Papers overview

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Review
2012
Review
2012
Axenfeld-Rieger syndrome is a genetic disease affecting multiple organ systems. In the eye, this condition manifests with varying… (More)
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2001
2001
PURPOSE Rieger syndrome is an autosomal dominant condition defined by anterior segment dysgenesis in combination with facial… (More)
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2001
2001
Mutations in the PITX2 bicoid-like homeobox gene cause Rieger syndrome. Rieger syndrome is an autosomal-dominant human disorder… (More)
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Highly Cited
2000
Highly Cited
2000
Mutations in the forkhead-like 7 (FKHL7) gene have been recently shown to cause juvenile glaucoma and anterior segment anomalies… (More)
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Highly Cited
1999
Highly Cited
1999
Rieger syndrome, an autosomal dominant disorder, includes ocular, craniofacial and umbilical abnormalities. The pitx2 homeobox… (More)
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Highly Cited
1999
Highly Cited
1999
Pitx2 is a homeodomain transcription factor that is mutated in Rieger syndrome, a haploinsufficiency disorder affecting eyes and… (More)
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Highly Cited
1999
Highly Cited
1999
Pitx1 (refs 1,2,3) and Pitx2 (refs 4, 5) are highly homologous, bicoid-related transcription factors. Pitx2 was initially… (More)
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Highly Cited
1996
Highly Cited
1996
Rieger syndrome (REG) is an autosomal–dominant human disorder that includes anomalies of the anterior chamber of the eye, dental… (More)
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Highly Cited
1996
Highly Cited
1996
Rieger syndrome is a genetically and phenotypically heterogeneous disorder typically characterized by malformations of the eyes… (More)
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1978
1978
Fourteen patients with hypodontia and the ocular features of the Rieger syndrome were examined for the presence of systemic… (More)
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