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A case of autosomal dominant optic atrophy

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Author:
No author available
Journal Title:
China Medicine
Issue:
8
DOI:
10.3760/j.issn.1673-4777.2024.08.025
Key Word:
视神经萎缩;遗传性;常染色体显性;Optic atrophy;Hereditary;Autosomal dominant

Abstract: This article reports a case of autosomal dominant optic atrophy to provide a reference for the clinical diagnosis of this type of disease.The patient had poor vision in both eyes without any obvious cause,and was diagnosed with autosomal dominant optic atrophy after combining auxiliary examinations and genetic testing.There is currently no effective treatment for this disease,and the key to treatment is to improve the patient's visual quality.Lifestyle changes and regular follow-up examinations are usually recommended.

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