Natalio J. Izquierdo

San Juan, Puerto Rico

Last Updated: 09/26/2026

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Found 67 publications

Usher Syndrome Type 2D Associated With a Novel Homozygous Whrn c.74dup Variant: A Case Report.

Usher Syndrome Type 2D Associated With a Novel Homozygous Whrn c.74dup Variant: A Case Report.

Journal: Cureus
Published: June 07, 2026

Stargardt Disease Presenting as Retinitis Pigmentosa: A Case of Monoallelic ABCA4-Associated Retinopathy.

Stargardt Disease Presenting as Retinitis Pigmentosa: A Case of Monoallelic ABCA4-Associated Retinopathy.

Journal: Cureus
Published: May 21, 2026

Clinical Validation of a CRX Variant Leading to a Cone-Rod Dystrophy.

Clinical Validation of a CRX Variant Leading to a Cone-Rod Dystrophy.

Journal: Cureus
Published: February 13, 2026

Retinal Degeneration and Visual Outcomes in Patients With Bardet-Biedl Syndrome: Genotypic Influences From a Caribbean Cohort.

Retinal Degeneration and Visual Outcomes in Patients With Bardet-Biedl Syndrome: Genotypic Influences From a Caribbean Cohort.

Journal: Cureus
Published: December 16, 2025

Rituximab-Based Management of Autoimmune Blistering Diseases: A Case Series Highlighting Ocular and Systemic Presentations.

Rituximab-Based Management of Autoimmune Blistering Diseases: A Case Series Highlighting Ocular and Systemic Presentations.

Journal: Cureus
Published: November 08, 2025

AptheraTM Intraocular Lens in a Latino Population: A Case Series.

AptheraTM Intraocular Lens in a Latino Population: A Case Series.

Journal: Cureus
Published: November 05, 2025

Clinical and Genetic Findings in an Autosomal Dominant Optic Atrophy-Compatible Phenotype Harboring an OPA1 Variant: A Case Report.

Clinical and Genetic Findings in an Autosomal Dominant Optic Atrophy-Compatible Phenotype Harboring an OPA1 Variant: A Case Report.

Journal: Cureus
Published: October 28, 2025

Ocular Findings in Siblings With Alagille Syndrome: A Report of Two Cases.

Ocular Findings in Siblings With Alagille Syndrome: A Report of Two Cases.

Journal: Cureus
Published: October 23, 2025

Hemoglobin C Disease With Splenomegaly and With Factor II Mutation Gene Thrombophilia: A Case Report.

Hemoglobin C Disease With Splenomegaly and With Factor II Mutation Gene Thrombophilia: A Case Report.

Journal: Cureus
Published: September 09, 2025

Sveinsson Chorioretinal Atrophy: A New Gene Variant.

Sveinsson Chorioretinal Atrophy: A New Gene Variant.

Journal: Cureus
Published: August 19, 2025

Retinitis Pigmentosa in a Patient With a Homozygous Mutation in the RBP3 Gene: A Case Report.

Retinitis Pigmentosa in a Patient With a Homozygous Mutation in the RBP3 Gene: A Case Report.

Journal: Cureus
Published: July 26, 2025

Analysis of the Body Mass Index of Latino Patients With Bardet-Biedl Syndrome.

Analysis of the Body Mass Index of Latino Patients With Bardet-Biedl Syndrome.

Journal: Cureus
Published: June 25, 2025
Showing 1-12 of 67

Last Updated: 09/26/2026