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Alexander Disease.

Ali Tavasoli1,2, Thais Armangue1,3,4, Cheng-Ying Ho5

  • 11 Division of Neurology, Center for Neuroscience and Behavioral Medicine, Children's National Health System, Washington, DC, USA.

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|January 24, 2017
PubMed
Summary
This summary is machine-generated.

Alexander disease, a genetic leukodystrophy, can mimic brain tumors. Early diagnosis is crucial, as genetic testing confirmed Alexander disease in an infant misdiagnosed with chiasmatic astrocytoma.

Area of Science:

  • Neurogenetics
  • Pediatric Neurology
  • Neuroradiology

Background:

  • Alexander disease is a rare, inherited leukodystrophy.
  • It results from mutations in the glial fibrillary acidic protein (GFAP) gene.

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