Repercusiones oculares del Síndrome de Alport: A propósito de dos casos

• Autores: Alex Jones, Manuel Gallegos, Ignacio Díaz, Magdalena Reyes, Sergio Zacharias
• Localización: Revista Médica de Chile, ISSN-e 0034-9887, Vol. 147, Nº. 4, 2019, págs. 522-526
• Idioma: español
• Títulos paralelos:
  • Alport syndrome. Report of two cases
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• Resumen

  • 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.