Structured Summary
Abstract
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.
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Synonyms
11 entry terms
- Fundus Flavimaculatus
- Stargardt Macular Degeneration
- Degeneration, Stargardt Macular
- Macular Degeneration, Stargardt
- Stargardt Macular Degenerations
- Juvenile Macular Degeneration
- Macular Degeneration, Juvenile
- Macular Dystrophy With Flecks, Type 1
- Stargardt Disease 1
- Degeneration, Juvenile Macular
- Juvenile Macular Degenerations
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2020(2010)
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AMA Style
References
- National Library of Medicine. Stargardt Disease. Medical Subject Headings (MeSH). 2026. Unique ID D000080362. http://id.nlm.nih.gov/mesh/2026/D000080362
- Stargardt Disease. In: Wikipedia. https://en.wikipedia.org/wiki/Stargardt_disease
- Stargardt Disease. In: Wikidata. https://www.wikidata.org/wiki/Q1317319