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Repercusiones oculares del Síndrome de Alport: A propósito de dos casos / Alport syndrome. Report of two cases
Jones, Alex; Gallegos, Manuel; Díaz, Ignacio; Reyes, Magdalena; Zacharias, Sergio.
  • Jones, Alex; Fundación Oftalmológica de Los Andes. Santiago. CL
  • Gallegos, Manuel; s.af
  • Díaz, Ignacio; Hospital Dr. Sótero del Río. Santiago. CL
  • Reyes, Magdalena; s.af
  • Zacharias, Sergio; Fundación Oftalmológica de Los Andes. Santiago. CL
Rev. méd. Chile ; 147(4): 522-526, abr. 2019. tab, graf
Article in Spanish | LILACS | ID: biblio-1014255
ABSTRACT
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.
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Full text: Available Index: LILACS (Americas) Main subject: Eye Diseases / Nephritis, Hereditary Type of study: Diagnostic study Limits: Adult / Humans / Male Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2019 Type: Article Affiliation country: Chile Institution/Affiliation country: Fundación Oftalmológica de Los Andes/CL / Hospital Dr. Sótero del Río/CL

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Full text: Available Index: LILACS (Americas) Main subject: Eye Diseases / Nephritis, Hereditary Type of study: Diagnostic study Limits: Adult / Humans / Male Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2019 Type: Article Affiliation country: Chile Institution/Affiliation country: Fundación Oftalmológica de Los Andes/CL / Hospital Dr. Sótero del Río/CL