Howell Neil, Miller Neil R, Mackey David A, Arnold Anthony, Herrnstadt Corinna, Williams Isla M, Kubacka Iwona
MitoKor, San Diego, California 92121, USA.
J Neuroophthalmol. 2002 Dec;22(4):262-9. doi: 10.1097/00041327-200212000-00002.
To report the clinical and mitochondrial genetic analyses of two families, each of which carries both the 11778 and 14484 Leber hereditary optic neuropathy (LHON) mutations in mitochondrial DNA.
In addition to detailed clinical histories, the complete sequence of the mitochondrial DNA (mtDNA) from each family was determined.
A small Australian LHON family (Vic20) and a family from the United States carry the 11778 and 14484 LHON mutations. In addition to the optic neuropathy, one branch of the Baltimore LHON pedigree had a high incidence of a fatal infantile encephalopathy. In both families, the 14484 LHON mutation was homoplasmic, whereas the 11778 LHON mutation was heteroplasmic.
There are no additional mtDNA sequence changes that explain the encephalopathy in the Baltimore LHON family, and a nuclear gene involvement is an alternative explanation that is supported by the available data. The ophthalmological characteristics and penetrance in the 11778 and 14484 "two-mutation" LHON families are not markedly more severe than those of classic LHON families who carry a single mtDNA mutation.
报告两个家族的临床及线粒体基因分析情况,这两个家族的线粒体DNA均携带11778和14484两种Leber遗传性视神经病变(LHON)突变。
除详细的临床病史外,还测定了每个家族线粒体DNA(mtDNA)的完整序列。
一个澳大利亚的小型LHON家族(Vic20)和一个来自美国的家族携带11778和14484 LHON突变。除视神经病变外,巴尔的摩LHON家系的一个分支中,致命性婴儿脑病的发病率很高。在这两个家族中,14484 LHON突变是同质性的,而11778 LHON突变是异质性的。
没有其他mtDNA序列变化可以解释巴尔的摩LHON家族中的脑病,核基因参与是一种有现有数据支持的替代解释。11778和14484“双突变”LHON家族的眼科特征及外显率并不比携带单个mtDNA突变的经典LHON家族明显更严重。