Concept information
Término preferido
Stargardt Disease
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Tipo
-
mesh:Descriptor
Definición
- A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases.
Concepto genérico
Etiquetas alternativas
- Fundus Flavimaculatus
- Stargardt Macular Degeneration
En otras lenguas
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francés
URI
http://data.loterre.fr/ark:/67375/JVR-Q1BLJG31-M
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