A novel adult case of juvenile-onset Alexander disease: complete remission of neurological symptoms for over 12 years, despite insidiously progressive cervicomedullary atrophy
We present here a 25-year-old woman with genetically confirmed (p.R276L mutation in the GFAP gene) juvenile-onset AxD. Episodic vomiting appeared at age nine, causing anorexia and insufficient growth. Brain MRI at age 11 showed a small nodular lesion with contrast enhancement in the left dorsal port...
Main Authors: | , , , , , , , , |
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Format: | Online |
Language: | English |
Published: |
Springer Milan
2011
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506840/ |