Amani S. Albakri

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

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Found 14 publications

Ophthalmic phenotype associated with a novel mutation in LAMB3 gene linked to uncommon Intermediate Junctional Epidermolysis Bullosa.

Ophthalmic phenotype associated with a novel mutation in LAMB3 gene linked to uncommon Intermediate Junctional Epidermolysis Bullosa.

Journal: American journal of ophthalmology case reports

Published: August 30, 2025

Profile of a large cohort of children with persistent fetal vasculature and their predictors of poor visual outcome in a tertiary eye hospital in Saudi Arabia.

Profile of a large cohort of children with persistent fetal vasculature and their predictors of poor visual outcome in a tertiary eye hospital in Saudi Arabia.

Journal: European journal of ophthalmology

Published: December 19, 2023

A Novel PGAP3 Gene Mutation-Related Megalocornea Can Be Misdiagnosed as Primary Congenital Glaucoma.

A Novel PGAP3 Gene Mutation-Related Megalocornea Can Be Misdiagnosed as Primary Congenital Glaucoma.

Journal: Cureus

Published: September 20, 2022

Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis.

Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis.

Journal: American journal of medical genetics. Part A

Published: September 14, 2022

Novel variant of KIF11 associated with MCLMR syndrome.

Novel variant of KIF11 associated with MCLMR syndrome.

Journal: Ophthalmic genetics

Published: August 25, 2022

Pediatric Retinal Detachment in Homozygous Protein C Deficiency: Genetic and Phenotypic Description of a Single Family.

Pediatric Retinal Detachment in Homozygous Protein C Deficiency: Genetic and Phenotypic Description of a Single Family.

Journal: Ophthalmic surgery, lasers & imaging retina

Published: May 16, 2022

Incidence and outcomes of microbial keratitis after cyclophotocoagulation to treat childhood refractory glaucoma.

Incidence and outcomes of microbial keratitis after cyclophotocoagulation to treat childhood refractory glaucoma.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: October 06, 2021

Retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome can be associated with coronary and major systemic arterial disease.

Retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome can be associated with coronary and major systemic arterial disease.

Journal: American journal of ophthalmology case reports

Published: December 17, 2020

Poretti-Boltshauser syndrome: a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration.

Poretti-Boltshauser syndrome: a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration.

Journal: Ophthalmic genetics

Published: November 30, 2020

Clinical features of LONP1-related infantile cataract.

Clinical features of LONP1-related infantile cataract.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: July 17, 2017

Biometry, optical coherence tomography, and further clinical observations in Knobloch syndrome.

Biometry, optical coherence tomography, and further clinical observations in Knobloch syndrome.

Journal: Ophthalmic genetics

Published: April 19, 2016

Regarding corneal decompensation in recessive cornea plana.

Regarding corneal decompensation in recessive cornea plana.

Journal: Ophthalmic genetics

Published: February 09, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026