Hodgson S, Child A, Dyson M
J Med Genet. 1987 Apr;24(4):210-4. doi: 10.1136/jmg.24.4.210.
We report a pedigree in which six males died of cardiac failure within the first eight months of life. These males were related through healthy females, as with X linked recessive inheritance. There was no consanguinity. None of the affected boys had an anatomical cardiac abnormality. In two affected brothers, histological evidence for endomyocardial fibroelastosis was documented, and in one of these electron microscopy demonstrated abnormalities of the mitochondria as found in mitochondrial cytopathy. A review of published reports revealed five similar X linked pedigrees, and in two of these mitochondrial abnormalities were found. We suggest that these families may show an X linked recessive cardiomyopathy with mitochondrial abnormalities.
我们报告了一个家系,其中六名男性在出生后的头八个月内死于心力衰竭。这些男性通过健康女性相互关联,符合X连锁隐性遗传模式。家系中无近亲结婚情况。所有患病男孩均无心脏解剖结构异常。在两名患病兄弟中,有心肌内膜纤维弹性组织增生的组织学证据,其中一人经电子显微镜检查发现存在线粒体细胞病中所见的线粒体异常。对已发表报告的回顾发现了另外五个类似的X连锁家系,其中两个家系也发现了线粒体异常。我们认为,这些家系可能表现为伴有线粒体异常的X连锁隐性心肌病。