Expanding the ABCD1 mutation spectrum: a novel variant in X-linked adrenomyeloneuropathy
The first reported case of AMN associated with the novel ABCD1 c.1922G > T (p.Gly641Val) variant is described, expanding the mutational spectrum of X-ALD.
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The first reported case of AMN associated with the novel ABCD1 c.1922G > T (p.Gly641Val) variant is described, expanding the mutational spectrum of X-ALD.
Potential causes of breakthrough ischemic stroke are identifiable in about half of breakthrough strokes and are associated with higher risk of recurrence compared with those without, warranting individualized approaches.
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