Hypometabolism and atrophy patterns associated with Niemann-Pick type C
Abstract Background Niemann–Pick disease type C (NP-C) is a rare genetic lysosomal lipid storage disorder characterized by progressive neurological impairment. Early diagnosis is critical for initiating treatment with miglustat, which can decelerate disease progression. In this study, we evaluated a...
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| Main Authors: | , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
SpringerOpen
2025-02-01
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| Series: | EJNMMI Research |
| Online Access: | https://doi.org/10.1186/s13550-025-01208-8 |
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