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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/23058
Title: The unique characteristics of Thai Leber hereditary optic neuropathy: Analysis of 30 G11778A pedigrees
Authors: Nopasak Phasukkijwatana
Wanicha L. Chuenkongkaew
Rungnapa Suphavilai
Bhoom Suktitipat
Sarinee Pingsuthiwong
Ngamkae Ruangvaravate
La Ongsri Atchaneeyasakul
Sukhuma Warrasak
Anuchit Poonyathalang
Thanyachai Sura
Patcharee Lertrit
Mahidol University
Keywords: Biochemistry, Genetics and Molecular Biology;Medicine
Issue Date: 1-Apr-2006
Citation: Journal of Human Genetics. Vol.51, No.4 (2006), 298-304
Abstract: Leber hereditary optic neuropathy (LHON) is characterized by acute or subacute bilateral visual loss, and affects mostly young males. The most common mitochondrial DNA mutation responsible for LHON worldwide is G11778A. Despite different genetic backgrounds, which are believed to influence the disease expression, most features of LHON are quite common in different populations. However, there seem to be a few ethnic-specific differences. Analyses of our 30 G11778A LHON pedigrees in Thailand snowed some characteristics different from those of Caucasians and Japanese. In particular, our pedigrees showed a lower male to female ratio of affected persons (2.6:1) and much higher prevalence of G11778A blood heteroplasmy (37% of the pedigrees contained at least one heteroplasmic G11778A individual). Heteroplasmicity seemed to influence disease manifestation in our patients but did not appear to alter the onset of the disease. The estimated overall penetrance of our G11778A LHON population was 37% for males and 13% for females. When each of our large pedigrees were considered separately, disease penetration varied from 9 to 45% between the pedigrees, and also varied between different branches of the same large pedigree. Survival analysis showed that the secondary LHON mutations G3316A and C3497T had a synergistic deleterious effect with the G11778A mutation, accelerating the onset of the disease in our patients. © The Japan Society of Human Genetics and Springer-Verlag 2006.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33646445329&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/23058
ISSN: 14345161
Appears in Collections:Scopus 2006-2010

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