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Interface in English. Medical references retain their original language; bilingual names and selected translations are provided.

中英关联术语

斯特格病

Stargardt Disease

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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.

中文名称索引;定义为 MeSH 英文原文,尚未逐条译审。MESH:D000080362 · MeSH 2026。

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