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Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.
Southeast Asian J Trop Med Public Health ; 2004 Mar; 35(1): 167-8
Article in English | IMSEAR | ID: sea-35227
ABSTRACT
A young Thai male presented with bilateral visual loss and disc pallor. The 14484 mutation responsible for Leber's hereditary optic neuropathy (LHON) was identified on blood mitochondrial analysis. His visual loss was more severe than the visual loss described in Caucasian and Japanese patients and showed no improvement. He had no other identifiable mutations related to LHON nor any associated neurological disorder. This is the first case report of LHON with the 14484 mutation in a Thai patient.
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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Thailand / Severity of Illness Index / Humans / Male / DNA, Mitochondrial / DNA Mutational Analysis / Follow-Up Studies / Point Mutation / Risk Assessment Type of study: Etiology study / Observational study / Prognostic study / Risk factors Country/Region as subject: Asia Language: English Journal: Southeast Asian J Trop Med Public Health Year: 2004 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Thailand / Severity of Illness Index / Humans / Male / DNA, Mitochondrial / DNA Mutational Analysis / Follow-Up Studies / Point Mutation / Risk Assessment Type of study: Etiology study / Observational study / Prognostic study / Risk factors Country/Region as subject: Asia Language: English Journal: Southeast Asian J Trop Med Public Health Year: 2004 Type: Article