X-Linked Infantile Nystagmus Latest Advances

Prevalence of foveal hypoplasia in a young adult cohort and its associations with visual acuity and birth parameters.

Journal: Strabismus

Published: August 19, 2026

Early Genotype-Driven Diagnosis of Hermansky-Pudlak Syndrome Type 4 in a Child With Oculocutaneous Albinism: An Ophthalmic Case Report.

Journal: Cureus

Published: August 07, 2026

Xq26.2 Contiguous Gene Deletion Involving FRMD7 and IGSF1: Highly Penetrant Infantile Nystagmus with Variable Endocrine Involvement.

Journal: Genes

Published: July 15, 2026

Ocular Nystagmus as the Initial Presenting Feature in a Patient with Complete CLTC Deletion: Expanding the Genotype-Phenotype Spectrum of CLTC-Related Disorder.

Journal: Genes

Published: July 09, 2026

Clinical features and genetic analysis for PAX6-associated ocular diseases

Journal: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology

Published: June 07, 2026

"Time to See" in Infantile Nystagmus.

Journal: Investigative ophthalmology & visual science

Published: May 07, 2026

Investigating How Brain Stimulation Mitigates Motion Sickness Using Spatiotemporal Nystagmus Parameters Captured in VR.

Journal: IEEE transactions on visualization and computer graphics

Published: April 06, 2026

The co-occurrence of homozygous variants in GUCY2D and MYO7A in Leber congenital amaurosis associated with deafness: clinical, molecular, and in silico investigation.

Journal: Molecular biology reports

Published: February 20, 2026

Recession-resection combined with vertical offset of horizontal rectus muscles for management of combined head turn and head tilt in idiopathic infantile nystagmus syndrome.

Journal: BMJ case reports

Published: February 05, 2026

Correction of Abnormal Head Position in Pediatric Nystagmus Using Yoked Low-Value Prism Glasses: A Retrospective Study.

Journal: Investigative ophthalmology & visual science

Published: February 02, 2026

Genetic Landscape and Clinical Characterization of FRMD7-Related Infantile Nystagmus Based on Large In-House Datasets and Literature Review.

Journal: Investigative ophthalmology & visual science

Published: January 14, 2026

Evaluation of the Child With Nystagmus: What to Do in the Age of Genetic Testing.

Journal: International ophthalmology clinics

Published: January 04, 2026

X-Linked Infantile Nystagmus Latest Advances

Find the Latest Research About X-Linked Infantile Nystagmus

Prevalence of foveal hypoplasia in a young adult cohort and its associations with visual acuity and birth parameters.

Prevalence of foveal hypoplasia in a young adult cohort and its associations with visual acuity and birth parameters.

Early Genotype-Driven Diagnosis of Hermansky-Pudlak Syndrome Type 4 in a Child With Oculocutaneous Albinism: An Ophthalmic Case Report.

Early Genotype-Driven Diagnosis of Hermansky-Pudlak Syndrome Type 4 in a Child With Oculocutaneous Albinism: An Ophthalmic Case Report.

Xq26.2 Contiguous Gene Deletion Involving FRMD7 and IGSF1: Highly Penetrant Infantile Nystagmus with Variable Endocrine Involvement.

Xq26.2 Contiguous Gene Deletion Involving FRMD7 and IGSF1: Highly Penetrant Infantile Nystagmus with Variable Endocrine Involvement.

Ocular Nystagmus as the Initial Presenting Feature in a Patient with Complete CLTC Deletion: Expanding the Genotype-Phenotype Spectrum of CLTC-Related Disorder.

Ocular Nystagmus as the Initial Presenting Feature in a Patient with Complete CLTC Deletion: Expanding the Genotype-Phenotype Spectrum of CLTC-Related Disorder.

Clinical features and genetic analysis for PAX6-associated ocular diseases

Clinical features and genetic analysis for PAX6-associated ocular diseases

"Time to See" in Infantile Nystagmus.

"Time to See" in Infantile Nystagmus.

Investigating How Brain Stimulation Mitigates Motion Sickness Using Spatiotemporal Nystagmus Parameters Captured in VR.

Investigating How Brain Stimulation Mitigates Motion Sickness Using Spatiotemporal Nystagmus Parameters Captured in VR.

The co-occurrence of homozygous variants in GUCY2D and MYO7A in Leber congenital amaurosis associated with deafness: clinical, molecular, and in silico investigation.

The co-occurrence of homozygous variants in GUCY2D and MYO7A in Leber congenital amaurosis associated with deafness: clinical, molecular, and in silico investigation.

Recession-resection combined with vertical offset of horizontal rectus muscles for management of combined head turn and head tilt in idiopathic infantile nystagmus syndrome.

Recession-resection combined with vertical offset of horizontal rectus muscles for management of combined head turn and head tilt in idiopathic infantile nystagmus syndrome.

Correction of Abnormal Head Position in Pediatric Nystagmus Using Yoked Low-Value Prism Glasses: A Retrospective Study.

Correction of Abnormal Head Position in Pediatric Nystagmus Using Yoked Low-Value Prism Glasses: A Retrospective Study.

Genetic Landscape and Clinical Characterization of FRMD7-Related Infantile Nystagmus Based on Large In-House Datasets and Literature Review.

Genetic Landscape and Clinical Characterization of FRMD7-Related Infantile Nystagmus Based on Large In-House Datasets and Literature Review.

Evaluation of the Child With Nystagmus: What to Do in the Age of Genetic Testing.

Evaluation of the Child With Nystagmus: What to Do in the Age of Genetic Testing.