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

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

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

Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling.

Journal: Scientific reports

Published: February 23, 2024

In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene.

Journal: Biochemical genetics

Published: February 07, 2024

Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2.

Journal: JCI insight

Published: November 01, 2023

Posterior embryotoxon as the initial ophthalmological sign of Axenfeld-Rieger syndrome.

Journal: Archivos de la Sociedad Espanola de Oftalmologia

Published: October 17, 2023

Alternative Genetic Diagnoses in Axenfeld-Rieger Syndrome Spectrum.

Journal: Genes

Published: September 23, 2023

Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome.

Journal: American journal of medical genetics. Part A

Published: August 28, 2023

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

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.

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.

Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling.

Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling.

In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene.

In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene.

Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2.

Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2.

Posterior embryotoxon as the initial ophthalmological sign of Axenfeld-Rieger syndrome.

Posterior embryotoxon as the initial ophthalmological sign of Axenfeld-Rieger syndrome.

Alternative Genetic Diagnoses in Axenfeld-Rieger Syndrome Spectrum.

Alternative Genetic Diagnoses in Axenfeld-Rieger Syndrome Spectrum.

Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome.

Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome.