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

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 abnorm...

Descripción completa

Guardado en:

Detalles Bibliográficos
Autores principales:	Jones,Alex, Gallegos,Manuel, Díaz,Ignacio, Reyes,Magdalena, Zacharias,Sergio
Lenguaje:	Spanish / Castilian
Publicado:	Sociedad Médica de Santiago 2019
Materias:	Lens Diseases Nephritis, Hereditary
Acceso en línea:	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000400522
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!

id	oai:scielo:S0034-98872019000400522
record_format	dspace
spelling	oai:scielo:S0034-988720190004005222019-08-14Repercusiones oculares del Síndrome de Alport: A propósito de dos casosJones,AlexGallegos,ManuelDíaz,IgnacioReyes,MagdalenaZacharias,Sergio Lens Diseases Nephritis, Hereditary 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.info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.147 n.4 20192019-04-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000400522es10.4067/S0034-98872019000400522
institution	Scielo Chile
collection	Scielo Chile
language	Spanish / Castilian
topic	Lens Diseases Nephritis, Hereditary
spellingShingle	Lens Diseases Nephritis, Hereditary Jones,Alex Gallegos,Manuel Díaz,Ignacio Reyes,Magdalena Zacharias,Sergio Repercusiones oculares del Síndrome de Alport: A propósito de dos casos
description	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.
author	Jones,Alex Gallegos,Manuel Díaz,Ignacio Reyes,Magdalena Zacharias,Sergio
author_facet	Jones,Alex Gallegos,Manuel Díaz,Ignacio Reyes,Magdalena Zacharias,Sergio
author_sort	Jones,Alex
title	Repercusiones oculares del Síndrome de Alport: A propósito de dos casos
title_short	Repercusiones oculares del Síndrome de Alport: A propósito de dos casos
title_full	Repercusiones oculares del Síndrome de Alport: A propósito de dos casos
title_fullStr	Repercusiones oculares del Síndrome de Alport: A propósito de dos casos
title_full_unstemmed	Repercusiones oculares del Síndrome de Alport: A propósito de dos casos
title_sort	repercusiones oculares del síndrome de alport: a propósito de dos casos
publisher	Sociedad Médica de Santiago
publishDate	2019
url	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000400522
work_keys_str_mv	AT jonesalex repercusionesocularesdelsindromedealportapropositodedoscasos AT gallegosmanuel repercusionesocularesdelsindromedealportapropositodedoscasos AT diazignacio repercusionesocularesdelsindromedealportapropositodedoscasos AT reyesmagdalena repercusionesocularesdelsindromedealportapropositodedoscasos AT zachariassergio repercusionesocularesdelsindromedealportapropositodedoscasos
_version_	1718437059645931520

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

Ejemplares similares