Repercusiones oculares del Síndrome de Alport: A propósito de dos casos.
Palabras clave:
Lens Diseases, Nephritis, HereditaryResumen
Alport syndrome is an inherited progressive form of glomerular disease that is often associated with sensorineural hearing loss and ocular abnormalities. We report two men with Alport syndrome. Both had chronic kidney disease and consulted for long-term loss of visual acuity. One had auditory abnormalities. On the ophthalmological examination, both had anterior lenticonus and one had dot or fleck retinopathy. Those findings are described in up to 50% and 70% of men with X-linked Alport syndrome, respectively. Both patients had a family history of Alport syndrome or suggestive signs and symptoms.Descargas
Publicado
2019-04-30
Cómo citar
Jones, A., Gallegos, M., Díaz, I., Reyes, M., & Zacharias, S. (2019). Repercusiones oculares del Síndrome de Alport: A propósito de dos casos. Revista Médica De Chile, 147(4). Recuperado a partir de https://revistamedicadechile.cl/index.php/rmedica/article/view/6726
Número
Sección
Reporte de Caso Clínico