Unusual macular thickness in Alport syndrome: case report


Autoria(s): Igami, Thais Z.; Lavezzo, Marcelo M.; Ferraz, Daniel A.; Takahashi, Walter Y.; Nakashima, Yoshitaka
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

29/10/2013

29/10/2013

2012

Resumo

This case report describes the presence of bilateral macular atrophy in a patient with Alport syndrome and compares this finding with literature. At fundoscopy, there was a discrete circumscribed macular thinning showing intense retinal pigment epithelium color and the presence of whitish circular retinal lesions ("dots" and "flecks") at nasal mid periphery of both eyes. Optical coherence tomography showed bilateral partial atrophy of the neurosensory retina in the macula, with a greater extent in the temporal region. This case describes a rare ophthalmological finding in Alport syndrome and important to be recognized for a precise diagnosis as well as for determining visual prognosis.

Identificador

ARQUIVOS BRASILEIROS DE OFTALMOLOGIA, SAO PAULO, v. 75, n. 4, supl., Part 3, pp. 283-285, JUL-AUG, 2012

0004-2749

http://www.producao.usp.br/handle/BDPI/36584

10.1590/S0004-27492012000400014

http://dx.doi.org/10.1590/S0004-27492012000400014

Idioma(s)

eng

Publicador

CONSEL BRASIL OFTALMOLOGIA

SAO PAULO

Relação

ARQUIVOS BRASILEIROS DE OFTALMOLOGIA

Direitos

openAccess

Copyright CONSEL BRASIL OFTALMOLOGIA

Palavras-Chave #NEPHRITIS, HEREDITARY/COMPLICATIONS #MACULA LUTEA/ABNORMALITIES #RETINAL DYSTROPHIES #RETINAL DISEASES/DIAGNOSIS #OPTICAL COHERENCE TOMOGRAPHY/INSTRUMENTATION #RETINOPATHY #OPHTHALMOLOGY
Tipo

article

original article

publishedVersion