Stargardt disease (Q99755): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1690038580 |
||
| 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. |
Statements
CID11:ID_1690038580
0 references
dki-india-ID_1690038580
0 references
Concluído
0 references
