Stargardt disease (Q99755): Difference between revisions
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CID11:ID_1690038580 | |||||||||||||||
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dki-india-ID_1690038580 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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Latest 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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| default for all languages | ID_1690038580 |
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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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CID11:ID_1690038580
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dki-india-ID_1690038580
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Concluído
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15 August 2026
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