Rare Diseases Symptoms Automatic Extraction

Infantile-onset Alexander disease: a genetically proven case with mild clinical course in a 6-year-old Indian boy.

[alexander disease]

Alexander disease is an autosomal dominant leukoencephalopathy characterized by developmental delay, macrocephaly, and characteristic neuroimaging abnormalities predominantly involving frontal lobes. We report a 6-year-old Indian boy with infantile-onset Alexander disease, who has an unusually mild clinical course and a de novo p.Leu359Val mutation in the glial fibrillary acidic protein gene.

Diseases presenting "fibrillary acidic protein gene" symptom

  • alexander disease

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