Monreal F J
Dev Med Child Neurol. 1985 Jun;27(3):325-30. doi: 10.1111/j.1469-8749.1985.tb04543.x.
Sixty-two patients with cerebral palsy seen consecutively in a pediatric neurology practice were submitted to a prospective protocol which tabulated their neurological findings, birth and developmental histories and an extensive neurodevelopmental pedigree. Their family histories were compared with those of three control groups, consisting of 62 children with headaches, 62 with school/behavior problems and 62 random normal children. The family histories of the cerebral-palsied children revealed an unusual number of relatives with cerebral palsy, mental retardation and seizures. This study suggests that a large proportion of cerebral-palsied individuals may be predisposed to aplasia/hypoplasia of neural tissue. Some affected by presumably static 'brain-damage' may in later years develop indolent degenerative disease. Indirect genetic factors may also play a major predisposing role in cerebral palsy of proven postnatal/perinatal onset.
在一家儿科神经科诊所连续就诊的62例脑瘫患者接受了一项前瞻性方案,该方案将他们的神经学检查结果、出生和发育史以及详尽的神经发育谱系制成表格。将他们的家族史与三个对照组的家族史进行了比较,这三个对照组分别由62名头痛儿童、62名有学校/行为问题的儿童和62名随机选取的正常儿童组成。脑瘫儿童的家族史显示,患有脑瘫、智力迟钝和癫痫的亲属数量异常。这项研究表明,很大一部分脑瘫患者可能易患神经组织发育不全/发育不良。一些可能受假定的静态“脑损伤”影响的患者,在晚年可能会患上隐匿性退行性疾病。间接遗传因素在已证实的产后/围产期发病的脑瘫中也可能起主要的易患作用。