Trifiletti R, Parano E, Falsaperla R, Incorpora G
Department of Neurology, Neuroscience and Pediatrics, Cornell University Medical College, New York, NY 10021, USA.
Childs Nerv Syst. 1995 Aug;11(8):453-5. doi: 10.1007/BF00334964.
A large Sicilian kinship in which myotonic dystrophy (DM) affected spanning four generations is presented. The pedigree clearly illustrates the phenomenon of anticipation, and illustrates that this phenomenon is more marked when transmission occurs through an affected female rather than an affected male. The pedigree is interpreted in light of recent genetic advances in DM. Neurosurgeons and neurologists should consider a diagnosis of DM when asked to evaluate a floppy infant with enlarged lateral ventricles, and should be aware of special features regarding its inheritance pattern.
本文介绍了一个大型西西里家族,其中强直性肌营养不良(DM)影响了四代人。系谱清楚地说明了遗传早现现象,并表明当通过患病女性而非患病男性进行遗传时,这种现象更为明显。根据DM最近的遗传学进展对该系谱进行了解释。神经外科医生和神经科医生在被要求评估侧脑室扩大的松软婴儿时应考虑DM的诊断,并应了解其遗传模式的特殊特征。