Clinical and molecular characterization of familial exudative vitreoretinopathy associated with microcephaly

Medicine and Dentistry

• Familial Exudative Vitreoretinopathy 100%
• Microcephaly 100%
• Family 100%
• Whole Genome Sequencing 50%
• Exome Sequencing 50%
• Sanger Sequencing 50%
• Patient 50%
• Low Density Lipoprotein Receptor Related Protein 5 33%
• Molecular Diagnosis 33%
• Family Counseling 16%
• Inpatient 16%
• Retinal Imaging 16%
• Pediatrics 16%
• Association 16%
• Child 16%
• Measurement 16%
• Genetic Heterogeneity 16%
• Angiogenesis 16%
• Clinical Assessment 16%
• Rod-Cone Dystrophy 16%
• Low Vision 16%
• Diagnosis 16%
• Learning Disorder 16%
• Nystagmus 16%
• Bone Density 16%
• Amaurosis 16%
• Atrophy 16%
• Osteoporosis 16%
• Phenotype 16%