Congenital amusia-pathology of musical disorder

被引:0
|
作者
Szyfter, Krzysztof [1 ]
Wigowska-Sowinska, Jadwiga [2 ]
机构
[1] Polish Acad Sci, Inst Human Genet, Ul Strzeszynska 32, PL-60479 Poznan, Poland
[2] Poznan Univ Med Sci, Dept Dev Neurol, Poznan, Poland
关键词
Congenital amusia; Pathophysiology; Disconnection syndrome; Hereditary disorder;
D O I
10.1007/s13353-021-00662-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Amusia also known as tone deafness affects roughly 1.5% population. Congenital amusia appears from birth and lasts over life span. Usually, it is not associated with other diseases. Its link to hearing impairment has been definitively excluded. Neurobiological studies point to asymmetrical processing of musical signals in auditory cortex of left and right brain hemispheres. The finding was supported by discovering microlesions in the right-side gray matter. Because of its connection with asymmetry, amusia has been classified to disconnection syndromes. Alternatively to the neurobiological explanation of amusia background, an attention was turned to the significance of genetic factors. The studies done on relatives and twins indicated familial aggregation of amusia. Molecular genetic investigations linked amusia with deletion of 22q11.2 chromosome region. Until now no specific genes responsible for development of amusia were found.
引用
收藏
页码:127 / 131
页数:5
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