Early-onset severe rod-cone dystrophy in young children with RPE65 mutations

Medicine and Dentistry

• Patient 62%
• Infancy 37%
• Age 37%
• Vision 25%
• Visual Impairment 25%
• Leber Congenital Amaurosis 25%
• Gene 25%
• Child 25%
• Family 25%
• Childhood 25%
• Parent 25%
• Rod-Cone Dystrophy 25%
• Phenotype 12%
• Clinical Examination 12%
• Visual Acuity 12%
• Retina Dystrophy 12%
• Peripheral Vision 12%
• Photophobia 12%
• Congenital Nystagmus 12%
• Visual Field Test 12%
• Infant 12%
• Amaurosis 12%
• Illumination 12%
• Congenital Stationary Night Blindness 12%

Biochemistry, Genetics and Molecular Biology

• Mutation 100%
• RPE65 87%
• Infancy 37%
• Age 37%
• Nested Gene 25%
• Vision 25%
• Childhood 25%
• Allele 12%
• Phenotype 12%
• Illumination 12%
• Visual Acuity 12%
• Peripheral Vision 12%