Single mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO) and Kearns-Sayre syndrome (KSS) patients from a multiethnic Asian population

被引:0
作者
Chong, Jia-Woei [1 ]
Annuar, Azlina Ahmad [2 ]
Wong, Kum-Thong [3 ]
Thong, Meow-Keong [4 ]
Goh, Khean-Jin [1 ]
机构
[1] Univ Malaya, Dept Med, Div Neurol, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Fac Med, Dept Mol Med, Kuala Lumpur 50603, Malaysia
[3] Univ Malaya, Fac Med, Dept Pathol, Kuala Lumpur 50603, Malaysia
[4] Univ Malaya, Fac Med, Dept Pediat, Kuala Lumpur 50603, Malaysia
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DIRECT REPEATS; MUTATIONS;
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中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Mitochondrial DNA (mtDNA) deletions are a major cause of chronic progressive external ophthalmoplegia (CPEO) and Kearns-Sayre syndrome (KSS). We analyzed single mtDNA deletions in 11 CPEO and one KSS patients by means of Southern blot and long polymerase chain reaction (PCR) assays. The deletion sizes ranged from 3.4 kb to 6.9 kb whereas the heteroplasmy level varied from 18.8% to 85.5%. Two unique deletions sized 4320 bp and 4717 bp were found. This study represents the first genetic screen of mtDNA disorders in Malaysia, and it follows the data seen in other published reports on CPEO and KSS genetic aetiology.
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页码:27 / 36
页数:10
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