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Ebstein anomaly associated with retinal venular dilatation, migraine, and visual snow syndrome: a case report.
de Jong, P T V M; Thee, E F; Straver, B.
Afiliação
  • de Jong PTVM; Department of Ophthalmology, Amsterdam University Medical Center, AMC, Meibergdreef 9, 1105, AZ, Amsterdam, The Netherlands. p.dejong@nin.knaw.nl.
  • Thee EF; Department of Retinal Signal Processing, The Netherlands Institute of Neuroscience, KNAW, Amsterdam, The Netherlands. p.dejong@nin.knaw.nl.
  • Straver B; Department of Ophthalmology, Erasmus University Medical Center, Molewaterplein 40, 3015, GD, Rotterdam, The Netherlands.
BMC Ophthalmol ; 22(1): 75, 2022 Feb 14.
Article em En | MEDLINE | ID: mdl-35164715
BACKGROUND: To present a case with Ebstein anomaly, a rare congenital heart disorder, with ophthalmological and neurophthalmological signs and symptoms. To date, retinal venous dilatation and visual snow syndrome have not been previously been published in this anomaly. CASE PRESENTATION: A 10-year-old white girl was diagnosed with Ebstein anomaly. From age 12, she regularly suffered from migraines with auras and photophobia. At age 16 she started to see short-term bouts of white snow, that after a year were present all day. At age 20, she was found to have a decreased retinal arteriovenous ratio. CONCLUSIONS: Retinal arterial tortuosity and venular dilatation are common in congenital heart disease but have not been described in Ebstein anomaly, nor has the visual snow syndrome.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enxaqueca com Aura / Anomalia de Ebstein / Transtornos de Enxaqueca Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enxaqueca com Aura / Anomalia de Ebstein / Transtornos de Enxaqueca Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article