Miller G
Neuromuscular Research Institute of Western Australia.
Arch Dis Child. 1989 Apr;64(4):557-62. doi: 10.1136/adc.64.4.557.
The incidence of minor congenital anomalies was examined in 36 patients with ataxic cerebral palsy, in unaffected family members, and in 100 unrelated control subjects. None of the control subjects or family members had more than four anomalies, and 25 of 36 (69%) of the patients had more than four. The distribution of anomalies differed considerably, with 60% of the index cases having seven or more, and 94% of the controls having three or less. The number occurring in the patients was significantly more than in their relatives. Of the 25 patients with more than four anomalies, 16 (64%) had undergone potentially adverse perinatal or early postnatal events. Thus minor congenital anomalies were considerably more frequent in those with ataxic cerebral palsy than in related or unrelated control subjects. These anomalies may be markers of early prenatal factors that contributed to the adverse outcome either directly or by predisposing to perinatal difficulties.
对36例共济失调型脑瘫患者、未受影响的家庭成员以及100名无关对照者进行了轻微先天性异常的发生率检查。对照者或家庭成员中无一例有超过4种异常,而36例患者中有25例(69%)有超过4种异常。异常的分布有很大差异,60%的索引病例有7种或更多异常,94%的对照者有3种或更少异常。患者出现的异常数量明显多于其亲属。在25例有超过4种异常的患者中,16例(64%)经历了潜在的不良围产期或出生后早期事件。因此,共济失调型脑瘫患者的轻微先天性异常比相关或无关对照者更为常见。这些异常可能是早期产前因素的标志,这些因素直接或通过易导致围产期困难而导致了不良结局。