American Journal of Medical Genetics · 1986 · 47 citations · 15 references
MedicineNeurologyNeuroscienceNeurochemistryNeuropharmacologyNeuropsychiatryIron DeficiencyIron Deficiency DisordersNeurodegenerative DiseasesNeurodegenerative DisordersNeurotransmissionSeizure DisordersAmygdaloid NucleiAutopsy Findings InterpretationBrain Iron DeficiencyDopamine D2-like ReceptorsNeuropathologic Autopsy FindingsPreliminary Autopsy ReportSeizuresSerotonergic Circuits
Postmortem human brain analyses have been performed to further evaluate pathogenetic aspects of the Rett syndrome. While there are no significant abnormalities with respect to amino acid concentrations in putamen, caudate nucleus, red nucleus and thalamus, the concentration of kynurenine is increased in putamen, caudate nucleus, gl. pallidus, raphe and amygdaloid n. In contrast, serotonin and its metabolite 5-hydroxyindole acetic acid are below normal levels. D2-receptor number is decreased and there is a significant drop in the concentration of the iron-binding protein ferritin. It can be concluded, that reduction of D2-receptors is due to loss of cholinergic and GABA-ergic cell bodies in the striatum or may be a response to iron deficiency. Low serotonergic and high kynurenergic activity may be of pathogenetic importance in the frequently observed cerebral seizures in Rett syndrome.
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The determination of tryptophan in plasma, liver, and urine.
W D Denckla, Henry K. Dewey · PubMed · 1967 · 828 citations
REGIONAL DISTRIBUTION OF AMINO ACIDS IN HUMAN BRAIN OBTAINED AT AUTOPSY
Thomas L. Perry, K. Berry, Shirley Hansen et al. · Journal of Neurochemistry · 1971 · 274 citations
Handbook of Clinical Neurology
J. F. Boyd · Journal of Clinical Pathology · 1979 · 259 citations