BACKGROUND and OBJECTIVE: The aim of the study was to determine optical coherence tomography angiography (OCTA) findings and to identify mutations in the RS1 gene in a three-generation family with X-linked juvenile retinoschisis (XLRS). PATIENTS AND METHODS: Clinical and genetic assessments were performed in 12 family members. OCTA was performed at baseline (12 members including cases and carriers) and after acetazolamide administration (three cases). Twenty healthy subjects (20 eyes, controls) were chosen for comparison. Molecular genetic analysis of the RS1 gene was performed in all family members. RESULTS: Deep capillary plexus density was reduced in cases compared with controls (P < .01) and was negatively related with retinal th...
Abstract Background To describe the clinical phenotype and genetic cause underlying the disease path...
Purpose: To describe the natural course, phenotype, and genotype of patients with X-linked retinosch...
Purpose : Patients with X-linked retinoschisis (XLRS) presenting at end-stage of disease are difficu...
Francesco Stringa,1,2 Emmanouli Tsamis,1,3 Alessandro Papayannis,1 Katarzyna Chwiejczak,1 Assad Jali...
To describe the clinical characteristics of a Taiwanese family with X-linked retinoschisis (XLRS) an...
The aim of the present study was to report a novel mutation in the retinoschisin 1 (RS1) gene in a C...
Purpose. To explore the structural progression of X-linked retinoschisis (XLRS) in patients by using...
Purpose. To explore the structural progression of X-linked retinoschisis (XLRS) in patients by using...
Many mutations in the retinoschisis (RS1) gene have been identified, but there are limited clinical ...
X-linked juvenile retinoschisis (XLRS) is an X-linked hereditary retinal dystrophy characterized by ...
Juvenile X-linked retinoschisis (XLRS, MIM#312700) belongs to a group of the vitreoretinal dystrophi...
Purpose: To describe the clinical phenotype of X linked juvenile retinoschisis (XLRS) in 12 Chinese ...
Background: X-linked retinoschisis (XLRS) is a leading cause of juvenile macular degeneration associ...
To investigate how genotype is related to phenotype and document correlations of genotype-phenotype ...
Purpose: To describe the natural course, phenotype, and genotype of patients with X-linked retinosch...
Abstract Background To describe the clinical phenotype and genetic cause underlying the disease path...
Purpose: To describe the natural course, phenotype, and genotype of patients with X-linked retinosch...
Purpose : Patients with X-linked retinoschisis (XLRS) presenting at end-stage of disease are difficu...
Francesco Stringa,1,2 Emmanouli Tsamis,1,3 Alessandro Papayannis,1 Katarzyna Chwiejczak,1 Assad Jali...
To describe the clinical characteristics of a Taiwanese family with X-linked retinoschisis (XLRS) an...
The aim of the present study was to report a novel mutation in the retinoschisin 1 (RS1) gene in a C...
Purpose. To explore the structural progression of X-linked retinoschisis (XLRS) in patients by using...
Purpose. To explore the structural progression of X-linked retinoschisis (XLRS) in patients by using...
Many mutations in the retinoschisis (RS1) gene have been identified, but there are limited clinical ...
X-linked juvenile retinoschisis (XLRS) is an X-linked hereditary retinal dystrophy characterized by ...
Juvenile X-linked retinoschisis (XLRS, MIM#312700) belongs to a group of the vitreoretinal dystrophi...
Purpose: To describe the clinical phenotype of X linked juvenile retinoschisis (XLRS) in 12 Chinese ...
Background: X-linked retinoschisis (XLRS) is a leading cause of juvenile macular degeneration associ...
To investigate how genotype is related to phenotype and document correlations of genotype-phenotype ...
Purpose: To describe the natural course, phenotype, and genotype of patients with X-linked retinosch...
Abstract Background To describe the clinical phenotype and genetic cause underlying the disease path...
Purpose: To describe the natural course, phenotype, and genotype of patients with X-linked retinosch...
Purpose : Patients with X-linked retinoschisis (XLRS) presenting at end-stage of disease are difficu...