Patient with CADASIL - a diagnostic challenge
INTRODUCTION: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a genetically determined and hereditary cerebral small vessel disease caused by mutations in the NOTCH3 gene. The onset is in the 3rd and 4th decade of life and is preceded by leukod...
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| Main Authors: | , , |
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| Format: | Book |
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Śląski Uniwersytet Medyczny w Katowicach,
2023-09-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |