Calabresi P A, Silvestri G, DiMauro S, Griggs R C
Department of Neurology, University of Rochester Medical Center, New York.
Muscle Nerve. 1994 Aug;17(8):943-5. doi: 10.1002/mus.880170815.
A 66-year-old woman with hereditary deafness and multiple symmetric lipomas presented with ataxia, slight myopathy, and neuropathy. Molecular genetic analysis of mitochondrial DNA revealed the adenine to guanine transition at position 8344 in the tRNA gene for lysine that has been associated with the myoclonic epilepsy and ragged red fiber (MERRF) syndrome. The deafness was transmitted by the patient's father and may have been an unrelated autosomal defect rather than a paternally transmitted mitochondrial point mutation.
一名患有遗传性耳聋和多发性对称性脂肪瘤的66岁女性出现共济失调、轻度肌病和神经病变。线粒体DNA的分子遗传学分析显示,赖氨酸tRNA基因第8344位的腺嘌呤向鸟嘌呤转变,这与肌阵挛性癫痫伴破碎红纤维(MERRF)综合征有关。耳聋由患者父亲遗传,可能是一个无关的常染色体缺陷,而非父系遗传的线粒体点突变。