ALTERED NEUROCHEMICAL MARKERS IN RETTS SYNDROME

被引:69
|
作者
WENK, GL
NAIDU, S
CASANOVA, MF
KITT, CA
MOSER, H
机构
[1] JOHNS HOPKINS UNIV,NEUROMNEMON LAB,BALTIMORE,MD 21218
[2] JOHNS HOPKINS UNIV,DEPT PSYCHOL,BALTIMORE,MD 21218
[3] KENNEDY INST HANDICAPPED CHILDREN,BALTIMORE,MD
[4] NIMH,INTRAMURAL RES PROGRAM,WASHINGTON,DC 20032
[5] JOHNS HOPKINS UNIV HOSP,DEPT NEUROL & PEDIAT,BALTIMORE,MD 21205
[6] JOHNS HOPKINS UNIV,SCH MED,NEUROPATHOL LAB,BALTIMORE,MD 21205
[7] JOHNS HOPKINS UNIV,SCH MED,DEPT PATHOL,BALTIMORE,MD 21205
[8] NIMH,CLIN BRAIN DISORDERS BRANCH,WASHINGTON,DC 20032
关键词
D O I
10.1212/WNL.41.11.1753
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Rett's syndrome (RS) is a neurologic disorder associated with severe mental deficiency and neurologic manifestations of cortical and extrapyramidal origin. The present report is a preliminary postmortem brain study that compares the levels of endogenous biogenic amines and selected neurotransmitter receptors in five cases with RS and six normal controls of similar age. The level of choline acetyltransferase activity was reduced in several cortical and subcortical regions. Endogenous levels of dopamine in the superior frontal and superior temporal gyri, occipital cortex, and putamen were reduced. The changes in specific neurotransmitter markers, particularly those associated with the basal ganglia and cortex, may underlie the progressive deterioration in motor and cognitive function characteristic of this progressive disorder.
引用
收藏
页码:1753 / 1756
页数:4
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