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The Neuroradiologic Spectrum of Wolfram Syndrome

Year: 2025

Type: article

Abstract: A 34-year-old woman developed type 1 diabetes at age 9. Around age 16, she experienced progressive vision loss, followed by gradual sensorineural hearing loss at 24. Genetic testing revealed a WFS1 mutation, confirming Wolfram syndrome (WS), a rare autosomal recessive, progressive neurodegenerative disorder.WS is characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness-summarized by the acronym DIDMOAD.[1]

Source: Annals of Indian Academy of Neurology

DOI: 10.4103/aian.aian_800_25

Authors: Mimi Lam, Bhavesh Trikamji

Institutions: University of California, Riverside, University of California, Los Angeles

Language: English

Topic: Neurological diseases and metabolism

Subfield: Neurology

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: diamond

OpenAlex ID: W4417101600

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Cites: 2

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