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Late‐onset Hallervorden‐Spatz disease presenting as familial parkinsonism
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1985
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Late‐onset Hallervorden‐spatz DiseaseNeurological DisorderCorticobasal DegenerationPathologyNeurologyBrain PathologyNeuropathologyBrain AtrophyProgressive DementiaNeurodegenerationMovement DisordersNeurodegenerative DiseasesNeuroanatomyParkinson DiseaseMild TremorDegenerative DiseaseFrontotemporal DementiaNeuroscienceMedicine
We studied a 68-year-old man who died after 13 years of progressive dementia, rigidity, bradykinesia, mild tremor, stooped posture, slow and shuffling gait, dystonia, blepharospasm, apraxia of eyelid opening, anarthria, aphonia, and incontinence. At autopsy, he had generalized brain atrophy with large deposits of iron pigment in the globus pallidus, caudate, and substantia nigra. Axonal spheroids were found in the globus pallidus, substantia nigra, medulla, and spinal cord. The neurochemical analysis of the brain revealed marked loss of dopamine in the nigral-striatal areas, with relative preservation of dopamine in the limbic areas. This is the oldest case of familial Hallervorden-Spatz disease reported and the first with neurochemical analysis of the brain.