Abstract Background To describe the clinical and multimodal imaging findings of a Brazilian family with Best vitelliform macular dystrophy. Methods A retrospective chart review of a Brazilian family was conducted and complementary fundus images (color photography, autofluorescence, fluorescein angiography and optical coherence tomography) were analyzed. Results Seven patients had typical macular lesions at different stages of Best vitelliform macular dystrophy. Electrooculography was performed in two of them and showed abnormal Arden ratio. The pedigree strongly suggests an autosomal dominant inheritance. Low visual acuity was mainly associated with advanced age, retinal pigment epithelium atrophy, and photoreceptors damage. However, yellow...
A 13-year-old boy presented to our ophthalmology outpatient department with gradual loss of vision i...
PURPOSE: To describe the phenotype of Best vitelliform macular dystrophy (BVMD) and to evaluate geno...
AIM: Longitudinal course and genotype-phenotype correlation in patients and carriers with heterozygo...
PURPOSE. To analyze retinal structure and function in vitelliform macular dystrophy (VMD) due to mut...
SUMMARY Two patients with vitelliform macular lesions, normal EOG Arden ratios, and no family histor...
Aim To describe the clinical features of a case series of patients with unilateral vitelliform macul...
Bests disease is an autosomal dominant hereditary macular dystrophy characterized by the presence of...
\s=b\Three members of a family had multi-focal, macular and extramacular\p=m-\Best's vitellifor...
Introduction: Best disease or vitelliform macular dystrophy is a rare autosomal dominant disorder wi...
PURPOSE: To estimate the prevalence, genotype, and clinical spectrum of Best vitelliform macular dys...
OBJECTIVE: To describe the clinical and genetic findings in 15 patients with multifocal vitelliform ...
La distrofia macular viteliforme de Best es una distrofia hereditaria de la retina, caracterizada ...
SUMMARY We report the case of a 22-year-old white female who presented for a routine ocular examinat...
Adult-onset foveomacular vitelliform dystrophy is a rare disease. It shares heritance features with ...
Purpose: To present the clinical and electrophysiological findings in four members of a family with ...
A 13-year-old boy presented to our ophthalmology outpatient department with gradual loss of vision i...
PURPOSE: To describe the phenotype of Best vitelliform macular dystrophy (BVMD) and to evaluate geno...
AIM: Longitudinal course and genotype-phenotype correlation in patients and carriers with heterozygo...
PURPOSE. To analyze retinal structure and function in vitelliform macular dystrophy (VMD) due to mut...
SUMMARY Two patients with vitelliform macular lesions, normal EOG Arden ratios, and no family histor...
Aim To describe the clinical features of a case series of patients with unilateral vitelliform macul...
Bests disease is an autosomal dominant hereditary macular dystrophy characterized by the presence of...
\s=b\Three members of a family had multi-focal, macular and extramacular\p=m-\Best's vitellifor...
Introduction: Best disease or vitelliform macular dystrophy is a rare autosomal dominant disorder wi...
PURPOSE: To estimate the prevalence, genotype, and clinical spectrum of Best vitelliform macular dys...
OBJECTIVE: To describe the clinical and genetic findings in 15 patients with multifocal vitelliform ...
La distrofia macular viteliforme de Best es una distrofia hereditaria de la retina, caracterizada ...
SUMMARY We report the case of a 22-year-old white female who presented for a routine ocular examinat...
Adult-onset foveomacular vitelliform dystrophy is a rare disease. It shares heritance features with ...
Purpose: To present the clinical and electrophysiological findings in four members of a family with ...
A 13-year-old boy presented to our ophthalmology outpatient department with gradual loss of vision i...
PURPOSE: To describe the phenotype of Best vitelliform macular dystrophy (BVMD) and to evaluate geno...
AIM: Longitudinal course and genotype-phenotype correlation in patients and carriers with heterozygo...