Neurochemical abnorrnalities in a patient with ataxia‐ telangiectasia
- 1 February 1984
- journal article
- research article
- Published by Wolters Kluwer Health in Neurology
- Vol. 34 (2) , 187
- https://doi.org/10.1212/wnl.34.2.187
Abstract
Biochemical abnormalities found in autopsied brain of a patient with ataxia-telangiectasia are described. Neuropathologic changes were limited to the cerebellum and spinal cord. The atrophic cerebellum showed marked loss of Purkinje''s and granule cells, and moderate loss of stellate and basket cells. Glutamic acid content was markedly reduced, and taurine content somewhat reduced in the cerebellar cortex, while GABA content was greatly reduced in the dentate nucleus. GABA receptor binding was reduced by 70% in cerebellar cortex. Phosphoethanolamine content was greatly reduced in the cerebellar cortex and inferior olivary nucleus. This compound was also deficient in 10 other brain regions and was the only extracerebellar neurochemical abnormality observed.This publication has 7 references indexed in Scilit:
- Neurotransmitter amino acids in dominantly inherited cerebellar disordersNeurology, 1981
- Postmortem Changes of Amino Compounds in Human and Rat BrainJournal of Neurochemistry, 1981
- GAMMA-AMINOBUTYRIC ACID RECEPTOR-BINDING IN MAMMALIAN BRAIN - HETEROGENEITY OF BINDING-SITES1981
- Diagnostic considerations in ataxia-telangiectasia.Archives of Disease in Childhood, 1979
- Genetically determined immunodeficiency diseases (GDID) and malignancy: Report from the Immunodeficiency-Cancer RegistryClinical Immunology and Immunopathology, 1978
- Concentrations of glutamic acid in cerebellar cortex and deep nuclei of normal mice and weaver, staggerer and nervous mutantsBrain Research, 1978
- Distribution of several amino acids in regions of the cerebellum of the rat1Journal of Neurochemistry, 1977