Stroke-Like Episodes in PMM2-CDG: When the Lack of Other Evidence Is the Only Evidence
Phosphomannomutase 2 deficiency (PMM2-CDG) is the most frequent congenital disorder of glycosylation. PMM2-CDG patients develop chronic cerebellar atrophy as a neurological hallmark. However, other acute neurological phenomena such as stroke-like episodes (SLE), epilepsy, migraine, and cerebrovascul...
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| Format: | Book |
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Frontiers Media S.A.,
2021-10-01T00:00:00Z.
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A1234.567 |
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