Stargardt disease (Q99755): Difference between revisions

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Doença de Stargardt é uma forma de degeneração macular hereditária juvenil caracterizada por manchas arredondadas ou pisciformes amareladas discretas ao redor da mácula ao nível do epitélio pigmentar da retina (EPR). A doença de Stargardt é a distrofia macular hereditária mais comum.
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Stargardt's disease is a form of juvenile hereditary macular degeneration characterised by discrete yellowish round or pisciform flecks around the macula at the level of the retinal pigment epithelium (rpe). Stargardt's disease is the most common hereditary macular dystrophy.

Revision as of 16:25, 16 August 2026

Stargardt's disease is a form of juvenile hereditary macular degeneration characterised by discrete yellowish round or pisciform flecks around the macula at the level of the retinal pigment epithelium (rpe). Stargardt's disease is the most common hereditary macular dystrophy.
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    English
    Stargardt disease
    Stargardt's disease is a form of juvenile hereditary macular degeneration characterised by discrete yellowish round or pisciform flecks around the macula at the level of the retinal pigment epithelium (rpe). Stargardt's disease is the most common hereditary macular dystrophy.

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