REGIONAL CEREBRAL BLOOD-FLOW IN ANGELMAN SYNDROME

被引：3
|
作者：
GUCUYENER, K
GOKCORA, N
ILGIN, N
BUYAN, N
SAYLI, A
机构：
[1] GAZI UNIV,FAC MED,DEPT NUCL MED,ANKARA,TURKEY
[2] GAZI UNIV,FAC MED,DEPT MOLEC BIOL & GENET,ANKARA,TURKEY
来源：
EUROPEAN JOURNAL OF NUCLEAR MEDICINE | 1993年 / 20卷 / 07期
关键词：
ANGELMAN SYNDROME; SINGLE-PHOTON EMISSION TOMOGRAPHY; HYPOPERFUSION;
D O I：
10.1007/BF00176561
中图分类号：
R8 [特种医学]; R445 [影像诊断学];
学科分类号：
1002 ; 100207 ; 1009 ;
摘要：
A patient with typical features of Angelman syndrome - a genetically inherited disorder involving developmental delay, ataxia, episodes of paroxysmal laughter and brachiocephaly - was studied with single-photon emission tomography. Hypoperfusion found in the left frontal and left temporoparietal regions can provide insights into the functional cerebral pathology, which may be due to a disturbance of the developmental process related to a chromosomal abnormality.
引用
收藏
页码：645 / 647
页数：3
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