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Eur Neurol ; 17(4): 233-8, 1978.
Article in English | MEDLINE | ID: mdl-689048

ABSTRACT

The description is given of a structural and ultrastructural aspect of a cerebral biopsy specimen collected from a 17-year-old patient, with very frequent convulsive seizures, dementia, motor aphasia and spastic tetraparesis. The disease started at the age of 9 years and evolved very slowly. The morphologic diagnosis was neurolopidosis, the ultrastructural one was atypical juvenile lipofuscinosis, the electron microscopic aspect being identical to that of another 3 cases published in the literature: highly polymorphous membranogranulovesicular cytosomes.


Subject(s)
Lipidoses/pathology , Adolescent , Aphasia/pathology , Axons/ultrastructure , Brain/ultrastructure , Cytoplasm/ultrastructure , Cytoplasmic Granules/ultrastructure , Epilepsy/pathology , Humans , Lipidoses/classification , Lipofuscin , Male , Neurons/ultrastructure
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