Iridogoniodysgenesis Type 1 Latest Advances

Axenfeld Rieger Syndrome Presenting with Open Angle Glaucoma in an Adult Patient: A Case Report.

Journal: JNMA; journal of the Nepal Medical Association

Published: March 02, 2026

National protocol for the diagnosis and management of Axenfeld-Rieger syndrome: Summary for the primary care physician

Journal: Journal francais d'ophtalmologie

Published: November 23, 2025

Axenfeld-Rieger Syndrome: From Zebrafish Models to Clinical Outcomes.

Journal: American journal of ophthalmology

Published: October 11, 2025

A Case Report on Glaucoma and Anterior Segment Abnormalities in Axenfeld-Rieger Syndrome.

Journal: Annals of African medicine

Published: July 30, 2025

Surgical Outcomes in Axenfeld-Rieger Syndrome: A Multicenter Retrospective Analysis.

Journal: American journal of ophthalmology

Published: July 15, 2025

Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndrome.

Journal: European journal of human genetics : EJHG

Published: July 02, 2025

Cataract Surgery Outcomes in Patients With Axenfeld-Rieger Syndrome.

Journal: Cornea

Published: April 16, 2025

19-Year Follow-up on Patients with Axenfeld-Rieger Anomaly or Syndrome and Fuchs' Endothelial Dystrophy Including the 6th Generation in a Pedigree.

Journal: Klinische Monatsblatter fur Augenheilkunde

Published: January 27, 2025

Deletion of exon 4 of the PITX2 in a child with Axenfeld-Rieger syndrome.

Journal: Ophthalmic genetics

Published: November 26, 2024

In Vivo Assessment of Retinal Phenotypes in Axenfeld-Rieger Syndrome.

Journal: Investigative ophthalmology & visual science

Published: April 08, 2024

Unusual Posterior Capsular Pigmentation in Axenfeld-Rieger Anomaly.

Journal: Ophthalmology. Glaucoma

Published: March 13, 2024

A Novel Mutation of FOXC1 (P136L) in an Axenfeld-Rieger Syndrome Patient With a Systematized Delusion of Jealousy: A Case Report and Literature Review.

Journal: Molecular genetics & genomic medicine

Published: March 11, 2024

Iridogoniodysgenesis Type 1 Latest Advances

Find the Latest Research About Iridogoniodysgenesis Type 1

Axenfeld Rieger Syndrome Presenting with Open Angle Glaucoma in an Adult Patient: A Case Report.

Axenfeld Rieger Syndrome Presenting with Open Angle Glaucoma in an Adult Patient: A Case Report.

National protocol for the diagnosis and management of Axenfeld-Rieger syndrome: Summary for the primary care physician

National protocol for the diagnosis and management of Axenfeld-Rieger syndrome: Summary for the primary care physician

Axenfeld-Rieger Syndrome: From Zebrafish Models to Clinical Outcomes.

Axenfeld-Rieger Syndrome: From Zebrafish Models to Clinical Outcomes.

A Case Report on Glaucoma and Anterior Segment Abnormalities in Axenfeld-Rieger Syndrome.

A Case Report on Glaucoma and Anterior Segment Abnormalities in Axenfeld-Rieger Syndrome.

Surgical Outcomes in Axenfeld-Rieger Syndrome: A Multicenter Retrospective Analysis.

Surgical Outcomes in Axenfeld-Rieger Syndrome: A Multicenter Retrospective Analysis.

Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndrome.

Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndrome.

Cataract Surgery Outcomes in Patients With Axenfeld-Rieger Syndrome.

Cataract Surgery Outcomes in Patients With Axenfeld-Rieger Syndrome.

19-Year Follow-up on Patients with Axenfeld-Rieger Anomaly or Syndrome and Fuchs' Endothelial Dystrophy Including the 6th Generation in a Pedigree.

19-Year Follow-up on Patients with Axenfeld-Rieger Anomaly or Syndrome and Fuchs' Endothelial Dystrophy Including the 6th Generation in a Pedigree.

Deletion of exon 4 of the PITX2 in a child with Axenfeld-Rieger syndrome.

Deletion of exon 4 of the PITX2 in a child with Axenfeld-Rieger syndrome.

In Vivo Assessment of Retinal Phenotypes in Axenfeld-Rieger Syndrome.

In Vivo Assessment of Retinal Phenotypes in Axenfeld-Rieger Syndrome.

Unusual Posterior Capsular Pigmentation in Axenfeld-Rieger Anomaly.

Unusual Posterior Capsular Pigmentation in Axenfeld-Rieger Anomaly.

A Novel Mutation of FOXC1 (P136L) in an Axenfeld-Rieger Syndrome Patient With a Systematized Delusion of Jealousy: A Case Report and Literature Review.

A Novel Mutation of FOXC1 (P136L) in an Axenfeld-Rieger Syndrome Patient With a Systematized Delusion of Jealousy: A Case Report and Literature Review.