Clinical course of cone dystrophy caused by mutations in the RPGR gene

Keyphrases

• Clinical Course 100%
• Cone Dystrophy 100%
• RPGR Gene 100%
• Female Carrier 75%
• Visual Acuity 50%
• ORF15 50%
• Spectral Domain Optical Coherence Tomography (SD-OCT) 25%
• Visual Outcome 25%
• Medical Records 25%
• Late-onset 25%
• Fundus Autofluorescence 25%
• Visual Loss 25%
• Survival Analysis 25%
• Legally Blind 25%
• Electroretinography 25%
• Photopic 25%
• Fundus Photography 25%
• Full-field Electroretinography 25%
• Visual Prognosis 25%
• All-affected 25%
• Frameshift mutation 25%
• Cumulative Risk 25%
• Dark Adaptation 25%
• X-linked 25%
• Ophthalmoscopy 25%
• Color Vision Testing 25%
• Rod Photoreceptor 25%
• Goldmann Perimetry 25%
• Direct Sequencing 25%
• Scotopic Response 25%
• Small Families 25%
• Ocular Involvement 25%
• Non-carriers 25%
• Kaplan-Meier 25%
• Product-limit 25%
• Terminal Region 25%
• 3-terminal 25%

Medicine and Dentistry

• Disease Course 100%
• Cone Dystrophy 100%
• Visual Acuity 66%
• Electroretinography 66%
• Dark Adaptation 66%
• Optical Coherence Tomography 33%
• Disease 33%
• Medical Record 33%
• Fundus Photography 33%
• Autofluorescence 33%
• Photoreceptor 33%
• Visual Impairment 33%
• Ophthalmoscopy 33%
• Visual Field Test 33%
• Survival Analysis 33%
• Frameshift Mutation 33%
• Color Vision 33%
• Vision Test 33%

Biochemistry, Genetics and Molecular Biology

• Visual Acuity 100%
• Electroretinography 100%
• Dark Adaptation 100%
• Medical Record 50%
• Autofluorescence 50%
• Frameshift Mutation 50%
• Color Vision 50%