Alexander's Disease: Clues to Diagnosis

Author:

Pridmore Clare L.1,Baraitser Michael2,Harding Brian3,Boyd Stewart G.4,Kendall Brian5,Brett Edward M.1

Affiliation:

1. Department of Paediatric Neurology, The Hospital for Sick Children, Great Ormond Street, London, England

2. Department of Clinical Genetics, The Hospital for Sick Children, Great Ormond Street, London, England

3. Department of Histopathology, The Hospital for Sick Children, Great Ormond Street, London, England

4. Department of Clinical Neurophysiology, The Hospital for Sick Childrne, Great Ormond Street, London, England

5. Department of Radiology The Hospital for Sick Children, Great Ormond Street, London, England

Abstract

The clinical, radiologic, neurophysiologic, and pathologic findings in 10 children with histologically proven Alexander's disease are described, and the presence of two broad clinical subgroups is confirmed. Macrocephaly, regression, and seizures are found in the infantile form, whereas bulbar signs predominate the so-called juvenile form. None of the clinical or neurophysiologic findings is pathognomonic, and radiologic features suggesting the diagnosis are not present in all cases. However, the combination of abnormalities may suggest the diagnosis and justify histologic confirmation. ( J Child Neurol 1993;8:134-144).

Publisher

SAGE Publications

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

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