Catarata congénita en un paciente con aneuploidía cromosómica 47,XYY

Archivos de la Sociedad Española de Oftalmología - Tập 93 - Trang 303-306 - 2018
A. Medina-Andrade1, C. Villanueva-Mendoza1, S. Arenas2, V. Cortés-González1
1Asociación para Evitar la Ceguera en México, Institución de Asistencia Privada, Hospital Dr. Luis Sánchez Bulnes, Ciudad de México, México
2Laboratorio de Medicina Genómica, Instituto Nacional de Rehabilitación, Ciudad de México, México

Tài liệu tham khảo

Ross, 2012, Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XYY Klinefelter syndrome, Pediatrics, 129, 769, 10.1542/peds.2011-0719

Lepage, 2014, Brain morphology in children with 47 XYY syndrome: A voxel and surface-based morphometric study, Genes Brain Behav, 13, 127, 10.1111/gbb.12107

Lloyd, 1992, Neonatal cataract: Aetiology, pathogenesis and management, Eye, 6, 184, 10.1038/eye.1992.37

Rajavi, 2016, Long-term visual outcome of congenital cataract at a Tertiary Referral Center from 2004 to 2014, J Curr Ophthalmol, 27, 103, 10.1016/j.joco.2015.11.001

Witkin, 1976, Criminality in XYY and XXY men, Science, 193, 547, 10.1126/science.959813