Axenfeld–Rieger syndrome: orthopedic and orthodontic management in a pediatric patient: a case report
AP Cazzolla, NF Testa, F Spirito, M Di Cosola… - Head & Face …, 2022 - Springer
Abstract Axenfeld–Rieger Syndrome (ARS) is a rare autosomal dominant genetic disease
with considerable expressive variability, characterized by ocular and non-ocular …
with considerable expressive variability, characterized by ocular and non-ocular …
Axenfeld-Rieger syndrome: a novel histopathologic finding associated with corneal abnormalities
T Yu, Z Dai, R Peng, G Xiao, P Zhang, S Ma, J Hong - BMC ophthalmology, 2022 - Springer
Abstract Background Axenfeld-Rieger syndrome (ARS) is a rare kind of anterior segment
dysgenesis (ASD). The most common ocular features of ARS are posterior embryotoxon and …
dysgenesis (ASD). The most common ocular features of ARS are posterior embryotoxon and …
The rare Axenfeld–Rieger syndrome with systemic anomalies: A case report and brief review of literature
W Song, X Hu - Medicine, 2017 - journals.lww.com
Interventions: A pars plana vitrectomy was performed to manage the retinal detachment.
Outcomes: Her best-corrected visual acuity was slightly improved after surgery. Lessons …
Outcomes: Her best-corrected visual acuity was slightly improved after surgery. Lessons …
[HTML][HTML] Axenfeld-Rieger Syndrome
EA Zamora, B Salini - 2019 - europepmc.org
Objectives: Identify the etiology Axenfeld-Rieger syndrome. Describe the presentation of
Axenfeld-Rieger syndrome. Outline the treatment and management options available for …
Axenfeld-Rieger syndrome. Outline the treatment and management options available for …
Axenfeld‐Rieger syndrome combined with a foveal anomaly in a three‐generation family: a case report
K Gołaszewska, N Dub, E Saeed, Z Mariak… - BMC …, 2021 - Springer
Abstract Background Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant eye
disorder that can also affect other organs of the human body. The condition is primarily …
disorder that can also affect other organs of the human body. The condition is primarily …
Mutation survey of candidate genes and genotype–phenotype analysis in 20 Southeastern Chinese patients with Axenfeld–Rieger syndrome
X Wang, X Liu, L Huang, S Fang, X Jia, X Xiao… - Current Eye …, 2018 - Taylor & Francis
Purpose/aim of the study: To conduct a survey spectrum of the PITX2, FOXC1, and PRDM5
genes to reveal genotype–phenotype correlations in a cohort of Southeastern Chinese …
genes to reveal genotype–phenotype correlations in a cohort of Southeastern Chinese …
Axenfeld–Rieger Syndrome: Rare Case Presentation and Overview
Axenfeld–Rieger syndrome (ARS) is an extremely rare autosomal dominant disorder
characterized by ocular, craniofacial, dental and periumbilical abnormalities. We present a …
characterized by ocular, craniofacial, dental and periumbilical abnormalities. We present a …
Complete detachment of the Schwalbe's line in a case of Axenfeld-Reiger anomaly-A rare presentation
A Mitra, S Choudhury, S Sar, N Das… - Indian Journal of …, 2022 - journals.lww.com
Discussion ARS is a bilateral, heterogeneous condition and may include developmental
abnormalities of the angle, trabecular meshwork, and iris.[1] Correctopia, polycoria …
abnormalities of the angle, trabecular meshwork, and iris.[1] Correctopia, polycoria …
[HTML][HTML] Síndrome de Axenfeld-Rieger con glaucoma asociado
Y González Blanco, FY Fumero González… - Revista Cubana de …, 2022 - scielo.sld.cu
El síndrome de Axenfeld-Rieger es una enfermedad congénita que puede estar asociada a
glaucoma en el 50% de los casos. Por esta razón se describen un caso clínico con …
glaucoma en el 50% de los casos. Por esta razón se describen un caso clínico con …